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Southeast Asian J Trop Med Public Health ; 1997 ; 28 Suppl 3(): 106-9
Artigo em Inglês | IMSEAR | ID: sea-35020

RESUMO

A total of 50 patients and relatives were studied comprising 12 cases of compound heterozygosity of beta-Malay and beta + thalassemia, 10 cases of compound heterozygosity of beta-Malay and beta degree thalassemia, 10 cases of beta-Malay and HbE and 18 cases of beta-Malay heterozygosity. Patients with beta-Malay and HbE had very mild clinical symptoms or were asymptomatic of thalassemia disease in the absence of blood transfusion. Homozygosity of beta-Malay produce mild clinical symptoms of thalassemic disease with normal facial characteristics and were not transfusion dependent. Patients with beta-Malay and IVS 1 nt 5 (G-C) had severe clinical symptoms, and were transfusion dependent. Patients with beta-Malay and beta degree thalassemia had severe clinical symptoms, delayed weight and height in relation to age, were transfusion dependent and had classical features of thalassemic diseases.


Assuntos
Transfusão de Sangue , Hemoglobina E/genética , Hemoglobinas Anormais/genética , Heterozigoto , Homozigoto , Humanos , Tailândia , Talassemia beta/sangue
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