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Concomitant hypoparathyroidism, sensorineural deafness, and renal agenesis: a case of Barakat syndrome.
Ranjbar-Omrani, Gholamhossein; Zamiri, Nima; Sabayan, Behnam; Mohammadzadeh, Azam.
Affiliation
  • Ranjbar-Omrani G; Endocrinology and Metabolism Research Center, Nemazee Hospital, Shiraz University of Medical Sciences, Shiraz, Iran. dabbaghm@sums.ac.ir
Arch Iran Med ; 11(3): 337-40, 2008 May.
Article in En | MEDLINE | ID: mdl-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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hearing Loss, Sensorineural / Hypoparathyroidism / Kidney Type of study: Etiology_studies Limits: Adult / Female / Humans Language: En Journal: Arch Iran Med Year: 2008 Document type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hearing Loss, Sensorineural / Hypoparathyroidism / Kidney Type of study: Etiology_studies Limits: Adult / Female / Humans Language: En Journal: Arch Iran Med Year: 2008 Document type: Article Affiliation country: Iran