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Kenny-Caffey syndrome

rare

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

Identifiers
MONDO:0016516 Orphanet:2333
Part of
Primordial dwarfism and slender bone disorderSyndromic disease
Also known as
Kenny syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal dominant Kenny-Caffey syndrome
Autosomal recessive Kenny-Caffey syndrome

Rare disease

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