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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| Autor Principal: | |
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| Formato: | Artigo |
| Idioma: | Persa |
| Publicado: |
Qom University of Medical Sciences
2012-05-01
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| 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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