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.

Detalles Bibliográficos
Autores principales: El Jabbour, Tony, Aboursheid, Tarek, Keifo, Mohammad Baraa, Maksoud, Ismael, Alasmar, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065464/
https://www.ncbi.nlm.nih.gov/pubmed/24982829
http://dx.doi.org/10.4103/2231-0770.133340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065464/
https://www.ncbi.nlm.nih.gov/pubmed/24982829
http://dx.doi.org/10.4103/2231-0770.133340

Ejemplares similares