Haemoglobin SD disease--rare case of jaundice.
J Indian Med Assoc
; 110(7): 501-2, 2012 Jul.
Article
em En
| MEDLINE
| ID: mdl-23520682
ABSTRACT
A 15 years old Muslim female presented with moderate anaemia, mild jaundice and hepatosplenomegaly with no history of blood transfusion in the past. Routine examination was suggestive of haemolytic jaundice. High pressure liquid chromatography (HPLC) electrophoresis of the patient's blood showed haemoglobin (Hb) SD disease. As it is a double heterozygous disease, family screening was done. It showed that the father was sickle cell trait. Mother was Hb D trait. Both the brothers were sickle cell trait and the only sister was normal. Hb SD disease is a very rare variety of haemoglobinopathy and the case is presented here due to its rarity.
Buscar no Google
Base de dados:
MEDLINE
Assunto principal:
Traço Falciforme
/
Hemoglobina Falciforme
/
Hemoglobinas Anormais
/
Países em Desenvolvimento
/
Hemoglobinopatias
/
Anemia Falciforme
Idioma:
En
Ano de publicação:
2012
Tipo de documento:
Article