1.
Avicenna J Med
; 4(3): 74-6, 2014 Jul.
Artículo
en Inglés
| MEDLINE
| ID: mdl-24982829
RESUMEN
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.
