Concomitant hypoparathyroidism, sensorineural deafness, and renal agenesis: a case of Barakat syndrome.
作者信息
Ranjbar-Omrani Gholamhossein, Zamiri Nima, Sabayan Behnam, Mohammadzadeh Azam
机构信息
Endocrinology and Metabolism Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
出版信息
Arch Iran Med. 2008 May;11(3):337-40.
PMID:18426329
Abstract
Barakat syndrome, also known as hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome is an extremely rare congenital disorder. Different etiologies are described for the syndrome but the definite pathophysiology remains unclear. Hereby, we present a case of Barakat syndrome who was diagnosed on the basis of clinical and molecular data.
摘要
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