Kenny-Caffey Syndrome

Author:

Abdel-Al Yaser K.1,Auger Louise T.2,El-Gharbawy Fatma3

Affiliation:

1. Department of Pediatrics, Mubarak Al-Kabeer Hospital, University of Kuwait

2. Department of Pediatrics, Faculty of Medicine, University of Kuwait, P.O. Box 24923, 13110, Safat, Kuwait

3. Department of Radiology, Mubarak Al-Kabeer Hospital, University of Kuwait

Abstract

Kenny-Caffey Syndrome is a rare syndrome characterized by growth retardation, uniformly small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia possibly with tetany at an early age, hyperphosphatemia, ocular abnormalities, and normal intelligence. We report a child with Kenny-Caffey Syndrome and idiopathic hypoparathyroidism and present a review of the literature summarizing the reported cases of this rare syndrome.

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Kenny-Caffey Syndrome Type 2;Journal of Craniofacial Surgery;2020-04-16

2. Ophthalmologic Impairment and Intellectual Disability in a Girl Presenting Kenny-Caffey Syndrome Type 2;Journal of Pediatric Genetics;2020-01-06

3. Modeling congenital disease and inborn errors of development in Drosophila melanogaster;Disease Models & Mechanisms;2016-03-01

4. Oral manifestations of patients with Kenny–Caffey Syndrome;European Journal of Medical Genetics;2012-08

5. Genetic Disorders in Kuwait;Genetic Disorders Among Arab Populations;2010

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