GAREM

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Title: Garem: A Comprehensive Guide to a Rare Genetic Disease

Description:

Garem is an extremely rare genetic disorder that affects the development of the kidneys and urinary tract. It is caused by a mutation in the SIX5 gene and is characterized by abnormal kidney structure and function. The condition affects both males and females and can present a variety of symptoms depending on its severity.

Associated Diseases:

Garem is often associated with other developmental disorders, including:

• Renal hypoplasia: Underdevelopment of the kidneys
• Renal agenesis: Absence of one or both kidneys
• Vesicoureteral reflux: Backflow of urine from the bladder into the ureters
• Hydronephrosis: Swelling of the kidneys due to urine buildup

Did you Know ?

The incidence of Garem is estimated to be 1 in 1,000,000 newborns. This makes it an extremely rare disorder.