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A Deaf Child with Hypoparathyroidism: A Case Report

<p><strong><em>Background and Objectives:</em></strong><strong> </strong>HDR (hypoparathyroidism, deafness and renal dysplasia) is an autosomal dominant syndrome due to mutation in the glutamyl aminotransferase. We report a deaf child with hypoparathyroidism...

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Detalles Bibliográficos
Autor Principal: R Fallah
Formato: Artigo
Idioma:Persa
Publicado: Qom University of Medical Sciences 2012-05-01
Series:Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum
Acceso en liña:http://journal.muq.ac.ir/en/index.php/jmuqen/article/view/105
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