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Kenny-Caffey syndrome type 1

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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Detalhes bibliográficos
Main Authors: El Jabbour, Tony, Aboursheid, Tarek, Keifo, Mohammad Baraa, Maksoud, Ismael, Alasmar, Diana
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4065464/
https://ncbi.nlm.nih.gov/pubmed/24982829
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2231-0770.133340
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