Alpha-Thalassemia (Hemoglobin H Disease; Thalassemia-alpha)

A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.


Diagnosis and therapies

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Symptoms and diagnosis

Symptoms:

    

Wikipedia

Corneal hydropsCongenital pulmonary airway malformationথ্যালাসেমিয়া - উইকিপিডিয়া

More information

Reported cases - Summary of cases reported on this diseaseWHO - World Health OrganizationPubMed - A service of the National Library of Medicine and National Institutes of HealthMEDLINE - Literature from the National Library of MedicineMeSH - Medical Subject HeadingsDeCS - Health Sciences Descriptors

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