Avicenna Journal of Medicine (Jul 2014)

Kenny-Caffey syndrome type 1

  • Tony El Jabbour,
  • Tarek Aboursheid,
  • Mohammad Baraa Keifo,
  • Ismael Maksoud,
  • Diana Alasmar

DOI
https://doi.org/10.4103/2231-0770.133340
Journal volume & issue
Vol. 04, no. 03
pp. 74 – 76

Abstract

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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.

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