Kenny-Caffey syndrome

Kenny-Caffey syndrome is a rare genetic condition causing skeletal abnormalities.[1] Individuals with the condition have a shortened stature and thickened long bones. Hypocalcemia is also common.[2]

Kenny-Caffey syndrome
Other namesKenny syndrome

KCS is autosomal dominant and caused by a mutation in FAM111A.[2] It affects males and females in equal proportion.[1]

Treatment is based on symptoms.[1]

References
  1. "Kenny-Caffey Syndrome".
  2. "OMIM Entry - # 127000 - KENNY-CAFFEY SYNDROME, TYPE 2; KCS2". www.omim.org. Retrieved 13 March 2019.
Classification
External resources
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