Hb D Punjab - Alpha Thalassaemia Combination in a Turkish Family
| Autor: | Ayten Arcasoy, Ayhan O. Cavdar |
|---|---|
| Rok vydání: | 2009 |
| Předmět: |
Adult
Male Heterozygote congenital hereditary and neonatal diseases and abnormalities Pediatrics medicine.medical_specialty Turkey Turkish Hemoglobins Abnormal Iron Electrophoresis Starch Gel Erythrocytes Abnormal Alpha (ethology) Gastroenterology Hemoglobins Amino acid analysis Blood protein electrophoresis hemic and lymphatic diseases Internal medicine medicine Humans Child business.industry virus diseases Hematology Middle Aged Iron blood Blood Protein Electrophoresis eye diseases language.human_language Blood Cell Count Pedigree language Thalassemia Female business Severe anaemia |
| Zdroj: | Scandinavian Journal of Haematology. 13:313-319 |
| ISSN: | 0036-553X |
| DOI: | 10.1111/j.1600-0609.1974.tb00275.x |
| Popis: | Data are presented of a Turkish family in whom Hb D and alfa-thalassaemia were present. Hb D was identified as Hb D Punjab by amino acid analysis. The propositus had a combination of Hb D Punjab and alfa-thalassaemia disease and suffered from a rather severe anaemia, therefore, a possibility of hypersplenism in addition to hereditary haemoglobin defects was considered. |
| Databáze: | OpenAIRE |
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