Kenny-Caffey syndrome type 1.

ABSTRACT: Kenny-Caffey syndrome type 1 is a rare hereditary skeletal disorder. We present here a documented case of a 7-month-old girl with the characteristic symptoms of growth retardation, dysmorphic features, and hypoparathyroidism.

SUBMITTER: El Jabbour T 

PROVIDER: S-EPMC4065464 | biostudies-literature | 2014 Jul

REPOSITORIES: biostudies-literature