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Alpha thalassemia trait symptoms

Common symptoms for each type may include: Silent alpha thalassemia carrier. This type has no symptoms What if one parent has alpha thalassemia trait and the other parent is a silent carrier? If one parent has the cis form of alpha thalassemia trait (αα/--), and the other parent is a silent carrier (αα/α-), there is a 25 percent (1 in 4) chance with each pregnancy of having a child with hemoglobin H disease. People with hemoglobin H disease can have an enlarged spleen, low red blood cell. Alpha-thalassemia is a blood disorder that reduces the body's production of hemoglobin. Affected people have anemia, which can cause pale skin, weakness, fatigue, and more serious complications. Two types of alpha-thalassemia can cause health problems: the more severe type is known as Hb Bart syndrome; the milder form is called HbH disease

No symptoms —Silent carriers of alpha thalassemia generally have no signs or symptoms of the disorder. The body's hemoglobin works normally because the lack of alpha globin protein is minor. Mild anemia —People with alpha thalassemia trait may have no signs or symptoms, but mild anemia is common: Feeling tired or wea The symptoms of alpha-thalassemia are variable, according to the severity of disease. Alpha-thalassemia is caused by mutations in the HBA1 and/or HBA2 genes. We each have two copies of HBA1 and HBA2, for a total of four copies.. Babies with no working copies of the HBA1 or HBA2 genes have the most severe form, hemoglobin Bart syndrome. Symptoms begin prenatally and include swelling of the body. Alpha-thalassemia. Four genes are involved in making the alpha hemoglobin chain. You get two from each of your parents. If you inherit: One mutated gene, you'll have no signs or symptoms of thalassemia. But you are a carrier of the disease and can pass it on to your children. Two mutated genes, your thalassemia signs and symptoms will be mild.

β-Thalassemia Symptoms - Balancing Life with β-Tha

A person who has thalassemia trait may not have any symptoms at all or may have only mild anemia, while a person with thalassemia major may have severe symptoms and may need regular blood transfusions In people with the characteristic features of alpha thalassemia, a reduction in the amount of normal hemoglobin prevents enough oxygen from reaching the body's tissues. Affected individuals also have a shortage of red blood cells (anemia), which can cause pale skin, weakness, fatigue, and more serious complications People who have thalassemia produce fewer healthy hemoglobin proteins, and their bone marrow produces fewer healthy red blood cells. Thalassemias can cause mild or severe anemia and other complications that can occur over time (such as iron overload). Symptoms of anemia include fatigue, difficulty breathing, dizziness, and a pale skin tone Alpha Thalassemia Types, Diagnosis, and Treatment. Amber Yates, MD, is a board-certified pediatric hematologist and a practicing physician at Baylor College of Medicine. Alpha thalassemia is an inherited anemia where the body is unable to produce a normal amount of hemoglobin. Hemoglobin A (the major hemoglobin in adults) contains two alpha. People who have thalassemia trait (also called thalassemia minor) carry the genetic trait for thalassemia but do not usually experience any health problems except perhaps a mild anemia. A person may have either alpha thalassemia trait or beta thalassemia trait, depending upon which form of beta protein is lacking

Alpha Thalassemia Johns Hopkins Medicin

Thalassemia - Symptoms, Types, Diagnosis, and Prevention

The two types are alpha thalassemia and beta thalassemia. The terms alpha and beta refer to the part of the hemoglobin the person is lacking. There are also terms for how serious the thalassemia.. People who have alpha or beta thalassemia trait can have mild anemia. However, many people who have these types of thalassemia have no signs or symptoms. Mild anemia can make you feel tired. Mild anemia caused by alpha thalassemia trait might be mistaken for iron-deficiency anemia. Mild to Moderate Anemia and Other Signs and Symptoms Alpha thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body. In people with the characteristic features of alpha thalassemia, a reduction in the amount of hemoglobin prevents enough oxygen from reaching the body's tissues

Alpha Thalassemia Trait - St

  1. Thalassemia is a blood disorder in which the body makes an abnormal form of hemoglobin. Learn more about its symptoms and how it's diagnosed
  2. I have alpha thalassemia trait, which was diagnosed when I was expecting my first child. Many blood tests were done, and by the eighth month of my pregnancy, they declared that I am suggestive of alpha thalassemia. Fortunately, my husband was normal, so my children didn't weren't affected
  3. Children with alpha thalassemia trait and those who are silent carriers have no symptoms at all. Some of the more common symptoms of alpha thalassemia include: fatigue, weakness, or shortness of breath a pale appearance or a yellow color to the skin (jaundice

Silent carrier and alpha thalassemia trait Alpha thalassemia silent carrier and trait are not illnesses and will not make your child sick in any way. It is not expected that individuals with silent carrier and alpha thalassemia trait have fatigue Fatigue is a feeling of weariness, tiredness, or lack of energy. Fatigue can be a normal and. The presence of thalassemia minor (like sickle cell trait in Africa) afforded protection Alpha thalassemia is a disorder in which the alpha globin protein is underproduced. anemia (the most common type), sickle cell anemia, vitamin B12 anemia, pernicious anemia, and aplastic anemia. Symptoms of anemia may include fatigue, malaise, hair.

Alpha-thalassemia (α-thalassemia, α-thalassaemia) is a form of thalassemia involving the genes HBA1 and HBA2. Thalassemias are a group of inherited blood conditions which result in the impaired production of hemoglobin, the molecule that carries oxygen in the blood. Normal hemoglobin consists of two alpha chains and two beta chains; in alpha-thalassemia, there is a quantitative decrease in. The signs and symptoms of alpha thalassemia vary depending on the type that a child has and how severe it is. Children with alpha thalassemia trait have no symptoms at all. Some of the more common symptoms of alpha thalassemia include: fatigue, weakness, or shortness of breath; a pale appearance or a yellow color to the skin (jaundice) irritabilit

Less severe cases may not be noticeable until later in childhood or even until adulthood. The main health problems associated with thalassaemia are: anaemia - severe tiredness, weakness, shortness of breath, pounding, fluttering or irregular heartbeats (palpitations) and pale skin caused by the lack of haemoglobi People with alpha thalassemia may also experience chest pain, drowsiness, and dizziness. The other thalassemia symptoms observed in beta patients include jaundice, delayed growth (in kids. A child of two carriers has a 25 percent chance of receiving two trait genes and developing the disease, and a 50 percent chance of being a thalassemia trait carrier. Most individuals with alpha thalassemia have milder forms of the disease, with varying degrees of anemia. The most severe form of alpha thalassemia, which affects mainly. The anemia resulting from alpha thalassemia can cause children to grow more slowly and also can lead to delayed puberty. Symptoms. The signs and symptoms of alpha thalassemia vary depending on the type that a child has and how severe it is. Children with alpha thalassemia trait and those who are silent carriers have no symptoms at all As with alpha-thalassemia trait, beta-thalassemia minor may go undiagnosed because of the absence of more distinct symptoms. Though, slight anemia may develop, this may be misconstrued as iron deficiency anemia. With beta-thalassemia intermedia, the symptoms range from mild anemia to severe ones that require blood transfusions regularly

Approximately 5 percent of the world's population has a globin variant, but only 1.7 percent has alpha or beta thalassemia trait.2 Thalassemia affects men and women equally and occurs in. copies of chromosome 16 (alpha zero trait) and the other parent is a carrier of one faulty alpha globin gene.on one of their copies of chromosome 16 (alpha plust trait). There is one chance in four of having a child with a mild form of alpha thalassaemia, Haemoglobin H disease. The faulty alpha globin gene copies are indicated by a minus sign (- Mild forms of alpha thalassaemia are difficult to detect in adults. Since alpha thalassaemia existing with structural defects of the beta chain of haemoglobin may lead to decreased levels of the abnormal haemoglobin, we examined individuals having sickle-cell trait for the possible coexistence of alpha thalassaemia Thalassemia can be categorized into forms such as alpha, beta, e beta, sickle beta thalassemia, with each having a major, intermedia, minor/trait form. If you have thalassemia minor, you are just a classifier who bears the gene for the disease but have no symptoms. 3 Left unchecked, thalassemia symptoms can get more severe and cause other. People who have thalassemia trait (also called thalassemia minor) carry the genetic trait for thalassemia but do not suffer from any health problems except a mild anemia. A person may have either alpha thalassemia trait or beta thalassemia trait, depending upon which form of beta protein is absent

Thalassemia comes in various forms, some are far more serious than others and some people with other versions of the disorder can have terrible health problems. Thankfully Alpha Thalassemia Trait has pretty low-level symptoms. As an adult, I learned to cope and manage my low-level exhaustion and factored those symptoms into my lifestyle Alpha-thalassemia is a group of disorders of hemoglobin synthesis, caused by mutations or deletions in at least 1 of the 4 alpha-globin genes, leading to variably impaired alpha-globin chain production, with accumulation of the now excess and unpaired beta-globin chains Again, since there are no symptoms, an individual may not know they have the trait until they have a child born with thalassemia major, a severe form of the disease. If both parents have the thalassemia trait there is a 25% chance that their child could be born with thalassemia major Alpha (α) thalassemia is the most common inherited disorder of hemoglobin (Hb) worldwide and is caused by HBA1 and HBA2 gene variants.Decreased or absent synthesis of the hemoglobin (Hb) α chain results in clinical presentations ranging from asymptomatic silent carriers to severe anemia and fetal lethality

Alpha-thalassemia Genetic and Rare Diseases Information

  1. or. A person with beta thalassemia
  2. This condition is called alpha thalassemia trait (homozygous α + trait if the missing genes are on opposite chromosomes or heterozygous α0 trait if both missing genes are on the same chromosome). The anemia, which is mild and causes no symptoms, can be mistaken for iron deficiency anemia or beta thalassemia trait
  3. Alpha-thalassemia is a genetic condition characterized by microcytic hypochromic anemia (i.e., where the red blood cell counts and hemoglobin levels are low) varying from mild (e.g., almost no symptoms) to severe (e.g., a lethal form causing death in the newborn period). Alpha-thalassemia occurs more frequently in individuals with Mediterranean.
  4. The symptoms of alpha thalassemia depend on the type. Most silent carriers do not have symptoms. Children with alpha thalassemia trait or hemoglobin H disease may have symptoms that range from mild to severe

The alpha thalassemia (α-thalassemia) syndromes are a group of hereditary anemias of varying clinical severity. They are characterized by reduced or absent production of 1 or more of the globin chains of which human hemoglobin is composed. Workup in alpha thalassemia relies primarily on laboratory evaluation, hemoglobin electrophoresis, and. The Alpha Thalassemias vary in severity, this variation is due to the mutations that cause reduction in the production of alpha chains the most severe is known as hemoglobin Bart and this affects the baby inside the mother's womb causing intrauterine death and hydrops fetalis syndrome also called Hb Bart syndrome or Alpha Thalassemia Major Alpha Thalassemia Minor, also called Alpha Thalassemia Trait (2 genes affected). People who have alpha thalassemia trait have red blood cells that are smaller (microcytic) and paler (hypochromic) than normal, have a decreased MCV (mean corpuscular volume, a measurement of the average size of a single red blood cell), and have a mild chronic anemia Alpha Thalassemia occurs when the body is unable to produce alpha globin chains for hemoglobin. Each person has four genes for alpha globin. When one or more of the alpha globin genes are absent or defective, this can cause either mild to severe symptoms of Alpha Thalassemia. The different forms of Alpha Thalassemia include

Alpha thalassemia occurs when one or more of the 4 alpha-globin genes that make up part of the hemoglobin molecule are missing or damaged. There are 4 types of alpha thalassemia: Alpha thalassemia silent carrier. One gene is missing or damaged, and the other 3 are normal. Blood tests are often normal Alpha thalassemia. Silent carrier, which means you have a genetic mutation for alpha thalassemia, but it doesn't cause symptomatic anemia. Alpha thalassemia trait, which can cause mild anemia. Hb H disease, which causes mild to moderate anemia and an enlarged spleen (splenomegaly). Alpha thalassemia major, the most severe form of alpha. Beta-thalassemia trait, which is also sometimes referred to as beta-thalassemia minor, means a patient is a carrier of beta-thalassemia but does not have the disease itself. This is an inherited blood disorder, present from birth, affecting the formation of haemoglobin. Compared to beta-thalassemia, the symptoms are much milder and have. Thalassemia is a one of blood disorder inherited from the parents marked by a deficiency of hemoglobin and red blood cells in the body. This disease is inherited when one or both the parents are carriers or thalassemia. A thalassemia carrier is a person who carries defective genes but they have very few or no symptoms of the disease Thalassemia is a hemoglobinopathy that is among the most common inherited disorders of hemoglobin production. The normal adult hemoglobin molecule (Hb A) consists of 2 pairs of chains designated alpha and beta. Normal adult blood also contains ≤ 2.5% Hb A2 (composed of alpha and delta chains) and < 2% hemoglobin F (fetal hemoglobin), which has gamma chains in the place of beta chains

Alpha Thalassemia - St

Genetic counseling. Alpha-thalassemia is usually inherited in an autosomal recessive manner.. Hb Bart syndrome. At conception, each sib of a proband with Hb Bart syndrome has a 25% chance of having Hb Bart syndrome (e.g., --/--), a 50% chance of having α-thalassemia trait with deletion or inactivation of two α-globin genes in cis (e.g., --/αα), and a 25% chance of being unaffected and not. Silent alpha thalassemia carriers have no signs or symptoms of the disease, but are able to pass thalassemia on to their children. Two missing or mutated genes is a condition called alpha thalassemia minor or having alpha thalassemia trait Alpha thalassemia can be harmful to pregnant women. It can lead to a stillborn birth. Children who are born with thalassemia may show signs of the disease right away, or symptoms may appear later. Most signs and symptoms usually show up within the first 2 years of life

The symptoms most often start in childhood. Affected people are at increased risk for having a child with alpha thalassemia major. Alpha thalassemia carrier. There are 2 types of carriers: A carrier can have the trait. This means he or she has mild symptoms but can pass the gene on to children. A carrier may be silent The symptoms most often start in childhood. Affected people are at increased risk for having a child with alpha thalassemia major. Alpha thalassemia carrier.There are 2 types of carriers: A carrier can have the trait I am 23 obese women has low blood pressure 83/60 and has alpha thalassemia trait. How can I can increase my blood pressure. I am having some symptoms like tired ,blur vision. Cold hands and feet sometimes. Can a obese women have alpha thalassemia

Symptoms: What are the main symptoms of alpha-thalassemia

A trait carrier of thalassemia will always be a trait carrier. It is a genetic trait passed down from parents to children. Being a trait carrier is not contagious. Over two million people in the United States carry the genetic trait for thalassemia. There are two types of thalassemia trait: Alpha thalassemia trait and Beta thalassemia trait 2. This test is designed to detect carriers of alpha thalassemia. Alpha thalassemia refers to a group of blood disorders that results from deficiency of functional hemoglobin typically due to decrease in the production of alpha globin chains. Individuals generally have four copies of the alpha globin genes (2 copies of HBA1 and 2 copies of HBA2) Thalassemia is a medical condition in which the body makes less hemoglobin than usual. It causes anemia. There are four genes that contribute to the making of hemoglobin. Problems with these genes can cause thalassemia, but when only one of the four genes is affected, the individual has no symptoms and is known as having thalassemia trait

Thalassemia - Symptoms and causes - Mayo Clini

  1. The symptoms of alpha thalassemia depend on the type. Most silent carriers don't have symptoms. Children with alpha thalassemia trait or hemoglobin H disease may have symptoms that range from mild to severe
  2. Traits, yes: Because the Alpha and beta thalassemia gene mutations are common, it is possible for a baby to inherit one from mom and another from dad. The child could be trait in both Alpha and beta, or less likely, be disease in one and trait in the other.It is hard to imagine being disease in both and still survive
  3. Alpha Thalassemia Silent Carrier. Chromosome 16 gene deletions: 1 of 4; Alpha Thalassemia Trait (Alpha Thalassemia Minor) Chromosome 16 gene deletions: 2 of 4; Peripheral Smear shows microcytosis without Anemia; Mild symptoms. Hemoglobin Constant Spring. Reduced alpha globin output; Moderate to severe symptoms. Alpha Thalassemia Intermedi
  4. Thalassemia is an inherited blood disorder that reduces the production of functional hemoglobin (the protein in red blood cells that carries oxygen). This causes a shortage of red blood cells and low levels of oxygen in the bloodstream, leading to a variety of health problems. There are two main types of thalassemia, alpha thalassemia and beta thalassemia..
  5. Alpha-thalassemia (α-thalassemia) is a comprehensive group of hereditary anemias, which features two clinical types, the hemoglobin Bart's hydrops fetalis syndrome, abbreviated as Hb Bart, and the hemoglobin H (HbH) disease. Alpha-Thalassemia (Alpha Thalassemia): Read more about Symptoms, Diagnosis, Treatment, Complications, Causes and Prognosis
  6. Alpha thalassemia. Deletions of the HBA1 and/or HBA2 genes are the most common cause of alpha thalassemia. Rarely, mutations in or near these genes can also be responsible for the disease. The signs and symptoms of alpha thalassemia tend to be more severe when the disease results from mutations in the alpha-globin genes than when it is caused by deletions of these genes
  7. or or trait usually do not need blood transfusions because they either do not have anemia or have only a mild anemia. Many times people with thalassemia are prescribed a supplemental B vita

What is Thalassemia? CD

  1. or have mild or no symptoms, but they carry the genetic changes and can pass them on to their children. Thalassaemia
  2. Alpha Thalassemia Trait or Mild Alpha Thalassemia. In this condition, the lack of alpha protein is somewhat greater. Patients with this condition have smaller red blood cells and a mild anemia, although many patients do not experience symptoms. However, physicians often mistake mild alpha thalassemia for iron deficiency anemia and prescribe.
  3. Permanent Redirect.
  4. Individuals with this genotype are usually clinically normal. If this patient is symptomatic, he or she may have an additional, rare alpha-thalassemia mutation. If the partner of this patient is a carrier of alpha (zero)- Thalassemia, this couple is at risk of having a child affected by Hemoglobin H disease. Family studies may be indicated
  5. ed by the severity of your particular type of thalassemia and the treatment you require. Because thalassemia is a blood disorder, any organ can be affected
  6. Alpha-thalassemia is characterized by a deficit in the production of the α-globin chains of hemoglobin. Individuals who carry a mutation affecting α-globin genes on a single chromosome, associated with mild anemia are said to have 'silent' α-thalassemia (if one gene is involved) or α-thalassemia trait (when two genes are involved), while compound heterozygotes or homozygotes expressing.

Alpha Thalassemia: Read About This Trai

Thalassemia is an inherited blood disorder. It inhibits the production of hemoglobin and red blood cells. A person may have alpha or beta thalassemia, and symptoms depend on these types and how. Alpha-thalassemia minor or alpha-thalassemia trait (Two mutated genes), Here the deficiency of alpha protein causes either no symptoms or presents with only mild anemia. Hemoglobin H disease (Three mutated genes) your signs and symptoms will be moderate to severe, such as severe anemia and enlargement of the liver and spleen

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Thalassemia Blood Disorder: Symptoms, Treatments, Tests

Just got a letter in the mail that my baby girl carries the alpha thalassemia trait (BARTS). Curious if anyone else has any experience or knowledge about this blood disorder. Waiting for my husband to get home to call the counselor they referred us to. Any questions I should have ready Thalassemia alpha, another subgroup within this family of conditions, also has a minor form. Thalassemia alpha trait or thalassemia alpha minor involves inheriting some, but not all, of the defective genes. There are four separate alleles involved in the expression of thalassemia alpha. Someone who inherits one or two has thalassemia alpha minor Surgical care is not needed for silent carriers or persons with alpha thalassemia trait. However, splenectomy may be beneficial for some patients with HbH disease. [ 12 ] Usually, splenectomy is reserved for patients with symptoms of hypersplenism (as reflected by leukopenia, thrombocytopenia, and worsening anemia) or for patients who were. Alpha thalassemia is an inherited blood disorder. This means it is passed down through the parent's genes. It causes anemia in affected children. Anemia is a low red blood cell or low hemoglobin level. Hemoglobin is the part of red blood cells. It carries oxygen to organs, tissues, and cells. Alpha thalassemia affects the production of hemoglobin Thalassemia Minor. this lack glcå:.in ísernewhatgreater Patients bor. have red ceils end a ;ahemia. alttxyugh they do 'histake alpha for iron deficiety prescribe an Both alpha same chro- osorne in thófpair (tran

Alpha Thalassemia Types, Diagnosis, and Treatmen

In Thalassemia minor, the hemoglobin genes are inherited during conception, one from the mother (egg) and one from the father (sperm). People with a Thalassemia trait in one gene are known as carriers or are said to have thalassemia minor.The only way to know if you carry the Thalassemia trait is to have a special blood test called hemoglobin electrophoresis which can identify the gene The two major types of thalassemia, alpha or beta, are named after defects in the specific for alpha or beta globin. The signs and symptoms of thalassemia are related to the number of genes affected or absent, causing different degrees of anemia. People who have alpha or beta thalassemia trait may asymptomatic or have mild anemia

beta thalassemia in children | Patient Education

I have a thalassemia trait - Thalassemia

Alpha thalassemia is the most common form of thalassemia. Alpha thalassemia is an autosomal recessive disorder and the incidences of alpha thalassemia have increased in United States and other Western nations because of migration. The region's most commonly affected with Alpha-thalassemia are Southeast Asian descent, Sub-Saharan Africa and. There are four kinds of alpha thalassemia: Carrier. This is caused by one missing gene or gene change for alpha thalassemia. When this happens, your baby is a carrier. Carriers usually do not have symptoms, but they can pass the condition to their children. Alpha Thalassemia Minor/Bart's Hemoglobin (also called alpha thalassemia trait). This.

Alpha-Thalassemia: Causes, symptoms, types, diagnosis and

Thalassemia is an inherited disease, meaning that at least one of the parents must be a carrier for the disease. It is caused by either a genetic mutation or a deletion of certain key gene fragments. Alpha thalassemia is caused by alpha-globin gene deletion which results in reduced or absent production of alpha-globin chains. Alpha globin gene. Removal of two-genes results in alpha thalassemia trait (minor) with microcytosis and usually no anemia. The three-gene removal results in major production of hemoglobin H (HbH), which has four beta chains (beta4). Alpha thalassemia intermedia, also called as HbH disease, causes microcytic anemia, hemolysis, and splenomegaly Thalassemia trait ( -thalassemia minor). This is also called -thalassemia trait and arises from the loss of 2 -globin genes, resulting on 1 of 2 genotypes (aa/--, or a-/a-). There is a mild anemia present, and red blood cells are hypochromic and microcytic. Clinical symptoms are usually absen Beta Thalassemia A defect in the production of beta globin protein from the beta genes is the most common cause of beta thalassemia. Both globin genes are present in the cell, but fail to produce hemoglobin adequately (This contrasts with alpha thalassemia, below, in which one or more of the genes is actually missing from the cell)

Thalassaemia - Thalassaemia carriers - NH

Start studying Alpha Thalassemia. Learn vocabulary, terms, and more with flashcards, games, and other study tools. How does a pt with Thalassemia minima (or Silent Carrier, or Alpha Thalassemia Trait) present? Clinically and hematologically normal. What symptoms are commonly present at birth in a pt with HbH disease 28-40% in alpha-thalassemia trait and beta-thalassemia trait ; May fall to less than 10% in beta-thalassemia major . DIFFERENTIAL DIAGNOSIS. A characteristic feature of beta-thalassemia trait is elevation of the level of Hb A2. This minor hemoglobin accounts for only 2 or 3% of the total in normal red cells, but in thalassemia trait it may be. Hemoglobin constant spring is an inherited form of alpha thalassemia where one of the four alpha globin genes is mutated. It is an unusual form of the silent carrier that causes no symptoms. Alpha thalassemia trait (also known as mild alpha thalassemia) is an inherited form of alpha thalassemia causing mild anemia Note that alpha thalassemia major (Hb Bart) results in hydrops fetalis, and thus is not an adult disease process; β-Thalassemia Minor (β-Thalassemia Trait) Heterozygous for β-globin mutation; Mild microcytic anemia; Splenomegaly uncommon; Microcytosis, hypochromia, basophilic stippling on blood smear; Co clinical symptoms Thalassemia is microcytic-hypochromic anemia. It is caused by the decreased synthesis of 1 or several globin chains. Since globin synthesis is flawed, the disease is one of the so-called hemoglobinopathies. Depending on which globin chain is affected by the disorder, one speaks of α- or ß-thalassemia. Thalassemias are caused by gene mutations.

Alpha Thalassemia - NORD (National Organization for Rare

Alpha thalassemia minor or alpha thalassemia-1 trait are other terms for this condition. Thalassemia minor or trait: patients have mild symptoms and they usually don't need blood transfusions. (physio-pedia.com) Sometimes alpha thalassemia trait (or minor) can be identified on newborn screen But you are a carrier of the disease and can pass it on to your children. 2 mutated genes, your thalassemia signs and symptoms will be mild. This condition may be called alpha-thalassemia trait. 3 mutated genes, your signs and symptoms will be moderate to severe. 4 mutated genes Alpha thalassemia can be inherited as an autosomal recessive trait or can be the result of a mutation, specifically of chromosome 16p, thereby affecting alpha globin protein synthesis

Thalassemia drThalassemia - Wikipedia

The first type of alpha thalassemia minor (trait) is a carrier state with no anemia and no symptoms. The second type has slightly abnormal red cells but still no anemia. The third type of alpha thalassemias produces a mild anemia that generally doesn't lead to serious complications The anemia resulting from alpha thalassemia can cause children to grow more slowly and also ca nlead to delayed puberty. Symptoms The signs and symptoms of alpha thalassemia vary depending on the type that a child has and how severe it is. Children with alpha thalassemia trait have no symptoms at all Aug 26, 2017 - Explore Trish Callos's board Beta thalassemia on Pinterest. See more ideas about beta thalassemia, alpha thalassemia, beta Therefore, you are considered a silent alpha thalassemia carrier. 2 mutated genes.Symptoms are usually mild. Here, you are considered to have an alpha-thalassemia trait. Risk Factors for Thalassemia Family history of thalassemia. Thalassemia is passed from parents to children through mutated hemoglobin genes Alpha thalassemia minor (also called alpha thalassemia trait). This condition is caused by two missing genes or gene changes. This condition is caused by two missing genes or gene changes. Your child may not have signs or symptoms, or she may have mild anemia, which can make her feel tired