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Kenny-Caffey syndrome

MONDO:0016516

A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia.

Also known as: Kenny syndrome

39 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive Kenny-Caffey syndrome (4) Autosomal dominant Kenny-Caffey syndrome (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Syndromic disease (24) Human disease (14) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1) Disease by body system or component (0)
Trials to join now! 21 Not yet recruiting 6 Not yet finished but already full! 4 Completed 7 Terminated 1
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