Kenny-Caffey syndrome type 1.

Autor: El Jabbour T; Department of Anatomic Pathology, Faculty of Medicine, Lebanese University, Lebanon, Syria., Aboursheid T; Department of Pediatrics, Faculty of Medicine, Damascus, Syria., Keifo MB; Department of Pediatrics, Faculty of Medicine, Damascus, Syria., Maksoud I; Pediatrics University Hospital, Faculty of Medicine, Damascus University, Damascus, Syria., Alasmar D; Pediatric Endocrinology and Metabolic Diseases Unit, University Children Hospital, Faculty of Medicine, Damascus University, Damascus, Syria.
Jazyk: angličtina
Zdroj: Avicenna journal of medicine [Avicenna J Med] 2014 Jul; Vol. 4 (3), pp. 74-6.
DOI: 10.4103/2231-0770.133340
Abstrakt: 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.
Databáze: MEDLINE