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A case of homozygous sickle cell disease in Sri Lanka.
Ceylon Med J ; 1991 Dec; 36(4): 172-4
Article in English | IMSEAR | ID: sea-47847
ABSTRACT
An 11 year old Muslim boy with a 2 month history of fever, loss of appetite, pallor and abdominal distension, had hepato-splenomegaly. Haemoglobin electrophoresis showed the presence of haemoglobins S and F, with complete absence of haemoglobin A. The sickling test was positive. Marital consanguinity was present. In both parents, the sickling test was positive and haemoglobin electrophoresis showed the presence of haemoglobins A and S. This is the first report of homozygous sickle cell disease in Sri Lanka.
Subject(s)
Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Fetal Hemoglobin / Hemoglobin A / Hemoglobin, Sickle / Child / Incidence / Consanguinity / Anemia, Sickle Cell Type of study: Incidence study / Prognostic study Language: English Journal: Ceylon Med J Year: 1991 Type: Article

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Humans / Male / Fetal Hemoglobin / Hemoglobin A / Hemoglobin, Sickle / Child / Incidence / Consanguinity / Anemia, Sickle Cell Type of study: Incidence study / Prognostic study Language: English Journal: Ceylon Med J Year: 1991 Type: Article