Barakat Syndrome Treatment News and Symptoms Information

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.

See below for updated news and information regarding Barakat Syndrome including new medical research, treatment options and advancements. 

Latest Acrodermatitis Barakat Syndrome Treatment News and Research

No recent news regarding Barakat Syndrome is available. 

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