Results 81 to 90 of about 6,512 (195)

Spherocytosis as a manifestation of postabortal clostridium welchii infections

, 1954
Two cases of postabortal Clostridium welchii infection are presented, both of which showed spherocytosis as an outstanding finding. In the patient who recovered, differential smears before and after illness showed normal morphology of the red cells in ...
Hadley, G. Gordon, Ekroth, Richard D.
core   +1 more source

Hereditary spherocytosis.

, 2009
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminant hemolytic anemia.
Babadoko, AA, Hassan, A, Isa, AH, Abunimye, P   +3 more
core  

Hereditary Spherocytosis in a 27-Year-old Woman: Case Report [PDF]

, 2009
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminant hemolytic anemia.
Isa, A.H., Hassan, A., Babadoko, A.A., Abunimye, P.   +3 more
core   +1 more source

Complications of delayed diagnosis and challenges: successfully managed SPTB gene variant hereditary spherocytosis with hepatocellular jaundice—a case report

Journal of Medical Case Reports
Background Hereditary spherocytosis is a rare genetic disorder of the red blood cell membrane that is characterized by anemia, jaundice, and splenomegaly; however, in the absence of family history and with unusual clinical presentation, the diagnosis ...
Sintayehu Mekonnen, Dereje Adefris, Belete Shikuro, Abdi Bati, Daniel Azmeraw, Temesegen Kassa, Eliud Teshome, Hawi Farris   +7 more
doaj   +1 more source

Haemolysis and cation transport in hereditary spherocytosis. [PDF]

, 1971
Inherited forms of anaemia were only generally recognized at the turn of this century and Osler's textbook of Medicine (1893) lists only chlorosis and pernicious anaemia in his section on primary or essential anaemia.
Wiley, James Saville
core  

Aplastic crisis in a child with hereditary spherocytosis with a strong family history resolving with supportive care

, 2018
Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity. Clinical features range from asymptomatic to fulminant hemolytic anaemia.
Shankar Vangalpudi V., Balaji M. D., Vadlamudy Vinay   +2 more
core   +1 more source

Hematology case: hereditary spherocytosis

, 2013
Aplastic crisis by Parvovirus B19 in a patient with hereditary spherocytosis can produce an acute severe and eventually life-threatening anemia. The authors present a clinical case of a 14-year old boy, enhancing the importance of clinical evaluation ...
Costa, E, Cleto, E, Costa, M, Barbot, J, Guerra, I, Freitas, I   +5 more
core  

Human parvovirus infection and aplastic crisis in hereditary spherocytosis

Current Medicine Research and Practice, 2011
Parvovirus B19 is usually associated with an acute, self-limiting disease. In patients with congenital haemolytic anaemia, infection with this virus can cause an aplastic crisis.
A Gogia, A Kakar, S P Byotra, U Parakh, M Bhargava   +4 more
doaj  

Plenary Abstracts Session & Oral Presentations

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source