Chronic Hemolytic Anemia Associated with Thalassemia and Sickling Traits
نویسندگان
چکیده
منابع مشابه
Chronic hemolytic anemia associated with thalassemia and sickling traits.
By P5IILLIP STURGEON, M.1)., F1. ntvF Y A. IT No, M.I)., Pmn.1). .ND WII4LIAM N. \ALENTINE, MD. P O\VELL, RO1)ARTE AN1) NEEL’ recemstly desen-ibed ins detail a family of Sicilians amscestrv displayinsg both the sickle cell trait amid thalassemia minor; the first family displayinsg boths of thuese tm-aits d!es(’ribed ins thsis counmstmy. Ins one member of this family exhibit-mug a severe cisronu...
متن کاملTwo Cases of Chronic Hemolytic Anemia Associated with Spherocytosis
Two cases of hemolytic anemia with spherocytosis were investigated. lnspite of chronic hemolysis tl::crc was no radiological changes in flat bones. Management and entity of spherocytosis is discussed m detail in this paper.
متن کاملChronic acquired hemolytic anemia associated with hemoglobinuria and Raynaud's phenomena.
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملChronic Acquired Hemolytic Anemia Associated with Hemoglobinuria and Raynaud’s Phenomena
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملSickle cell anemia, thalassemia, and congenital hemolytic anemias
Each year, an estimated 300,000 infants are born with either of the two most common hemoglobinopathies: the sickle cell diseases or the thalassemias. These inherited diseases are the most prevalent monogenetic disorders worldwide. Sickle cell disease makes up 85% of the total infants, and thalassemias the remaining 15%. It is increasingly apparent that sickle cell disease and thalassemia have b...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Blood
سال: 1952
ISSN: 0006-4971,1528-0020
DOI: 10.1182/blood.v7.3.350.350