Literature DB >> 1725506

A case of homozygous sickle cell disease in Sri Lanka.

G N Lucas1, D R Jayawardena.   

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.

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Year:  1991        PMID: 1725506

Source DB:  PubMed          Journal:  Ceylon Med J        ISSN: 0009-0875


  1 in total

1.  Sickle cell disease in Sri Lanka: clinical and molecular basis and the unanswered questions about disease severity.

Authors:  Thamal Darshana; Dayananda Bandara; Upul Nawarathne; Udaya de Silva; Yasinta Costa; Kalavitigoda Pushpakumara; Sumithra Pathirage; Seuwandi Basnayake; Chamila Epa; Pradeepa Dilrukshi; Maheshaka Wijayawardena; Angela A Anthony; Rexan Rodrigo; Aresha Manamperi; Frances Smith; Angela Allen; Stephan Menzel; David Rees; Anuja Premawardhena
Journal:  Orphanet J Rare Dis       Date:  2020-07-06       Impact factor: 4.123

  1 in total

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