Outline of Diagnostic Dilemmas in Thalassaemia - Guidelines for …
WEBOf the multiple complaints patients with thalassaemia present with, unexplained abdominal pain spans a wide differential diagnosis including chloelythiasis, pancreatitis, portal vein thrombosis, hepatic capsule distention and kidney stones.
Alpha- and Beta-thalassemia: Rapid Evidence Review | AAFP
WEBThalassemia is a group of autosomal recessive hemoglobinopathies involving ineffective production of normal alpha- or beta-globin chains, which can lead to ineffective erythropoiesis, premature...
Thalassemia - Diagnosis & treatment - Mayo Clinic
WEBNov 17, 2021 · People with moderate to severe forms of thalassemia are usually diagnosed within the first two years of life. If you've noticed some of the signs and symptoms of thalassemia in your infant or child, see your family doctor or pediatrician.
Beta Thalassemia: Types, Symptoms & Treatment - Cleveland Clinic
WEBSwollen abdomen. Weak or misshapen bones in your arms, legs and face. Infants with moderate to severe beta thalassemia may be especially fussy and get frequent infections.
Thalassemia: Types, Traits, Symptoms & Treatment - Cleveland Clinic
WEBJun 3, 2022 · Beta thalassemia intermedia may cause mild anemia symptoms, or it may cause the following symptoms associated with more moderate disease: Growth problems. Delayed puberty. Bone abnormalities, such as osteoporosis. An enlarged spleen (the organ in your abdomen that plays a part in fighting infection).
Diagnosis of thalassemia (adults and children) - UpToDate
WEBApr 5, 2024 · Individuals with thalassemia have variable degrees of anemia and extramedullary hematopoiesis, which in turn can cause bone changes, impaired growth, and iron overload. This topic review discusses the clinical manifestations and diagnosis of alpha and beta thalassemia, the two most common forms.
Thalassemia - StatPearls - NCBI Bookshelf
WEBAug 8, 2023 · Thalassemia is a heterogeneous group of blood disorders affecting the hemoglobin genes and resulting in ineffective erythropoiesis. The decreased production of hemoglobin results in anemia in early age and frequent blood transfusions are required to keep up the hemoglobin levels.
Diagnosis and management of thalassaemia | The BMJ
WEBJan 25, 2012 · Antenatal prevention programmes consist of identifying and counselling couples who carry the relevant genes, and offering them different options to prevent having a child with thalassaemia. In this review we summarise diagnostic, treatment, and prevention options in thalassaemia for generalist readers.
Thalassemias - Thalassemias - MSD Manual Consumer Version
WEBThalassemias are a group of inherited disorders resulting from an imbalance in the production of one of the 4 chains of amino acids that make up hemoglobin (the oxygen-carrying protein found in red blood cells). Symptoms depend on the type of thalassemia. Some people have jaundice and abdominal fullness or discomfort.
Symptoms, diagnosis and treatment - BMJ Best Practice
WEBDec 6, 2023 · Beta-thalassaemia is an inherited microcytic anaemia caused by mutation (s) of the beta-globin gene leading to decreased or absent synthesis of beta-globin, resulting in ineffective erythropoiesis.
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