A first report on Hb Q-Iran in association with alpha-thalassemia in a case of spinal ischemia.
Clin Lab
; 57(3-4): 221-4, 2011.
Article
em En
| MEDLINE
| ID: mdl-21500730
ABSTRACT
BACKGROUND:
Hemoglobin Q-Iran is a rare variant which has not been described in association with alpha-thalassemia to date. We present the case of a Turkish patient who developed spinal ischemia.METHODS:
Spinal ischemia was diagnosed clinically, via magnetic resonance imaging and angiographically. Blood samples were analyzed by high performance liquid chromatography, electrophoresis, gene sequencing, hematological and biochemical analysis.RESULTS:
We detected hemoglobin Q-Iran in association with alpha-thalassemia. The same hemoglobinopathy was detected in two members of the patient's family.CONCLUSIONS:
As various differential diagnosis approaches failed to reveal the cause of spinal ischemia, the combined hemoglobinopathy was eventually postulated.
Buscar no Google
Base de dados:
MEDLINE
Assunto principal:
Hemoglobinas Anormais
/
Talassemia alfa
/
Isquemia do Cordão Espinal
Idioma:
En
Ano de publicação:
2011
Tipo de documento:
Article