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Congratulation to Margaret Chan Familial and Sporadic GJB2-Related Deafness in Iran: Review of Gene Mutations
Connexin 26 Deafness Autosomal recessive non syndromic hearing loss Iran
2007/1/20
Background: Mutations in the GJB2 gene encoding connexin 26 protein, are the main cause for autosomal recessive and sporadic non syndromic hearing loss in many populations. Here, we have taken togethe...
THIAMINE–RESPONSIVE MEGALOBLASTIC ANEMIA,SENSORINEURAL DEAFNESS AND DIABETES MELLITUS
Refractory anemia thiamine responsive
2004/10/31
The syndrome of diabetes mellitus, sensorineural deafness and megaloblastic anemia dose not result from thiamine deficiency. The previous reported patients had no sign of beriberi, had normal nutritio...