What is Barakat Syndrome?
(Symptoms, Causes & Treatment)
According to the Genetic and Rare Diseases Information Center, Barakat syndrome is a rare inherited condition which is characterized by hypoparathyroidism, sensorineural hearing loss, and renal (kidney) disease. Most cases have been attributed to a mutation on chromosome 10p which affects the GATA3 gene. Inheritance is likely autosomal dominant.
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Latest Acrodermatitis Barakat Syndrome Treatment News and Research
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