Alpha-thalassemia is a type of thalassemia that involves the HBA1 and HBA2 genes. This inherited blood disorder results from impaired production of...
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Congenital afibrinogenemia or familial afibrinogenemia is a rare, genetically inherited blood fibrinogen disorder in which the blood does not clot normally due...
Have you ever heard about Adult-Onset Still’s Disease (AOSD) or Wissler-Fanconi syndrome? If not, this short article would be a great...
Adenosine deaminase deficiency (ADA deficiency) is a rare disease with an incidence of <1 case per 100,000 live births worldwide,...
It is hard until now to answer this question! Despite that, no one can ignore our successful experience in using...
Acrospiroma (Know as Hidradenoma or Eccrine Acrospiroma) too, is a rare cutaneous tumor of the eccrine sweat gland which occurs primarily in adult...
REGN-COV is a combination of two monoclonal antibodies that work in reducing the infectivity of COVID-19. Until this movement the...
Acute myeloid leukemia (AML) is a rare type of cancer that affects the myeloid line of blood cells. AML is characterized...
Acute lymphoblastic leukemia (ALL) is a rare type of cancer that affects the lymphoid line of blood cells and characterized...
Acute intermittent porphyria (AIP) is a rare metabolic disorder that affects heme production as a result of porphobilinogen deaminase deficiency....
