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
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author El Jabbour, Tony
Aboursheid, Tarek
Keifo, Mohammad Baraa
Maksoud, Ismael
Alasmar, Diana
author_facet El Jabbour, Tony
Aboursheid, Tarek
Keifo, Mohammad Baraa
Maksoud, Ismael
Alasmar, Diana
author_sort El Jabbour, Tony
collection PubMed
description 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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spelling pubmed-40654642014-07-01 Kenny-Caffey syndrome type 1 El Jabbour, Tony Aboursheid, Tarek Keifo, Mohammad Baraa Maksoud, Ismael Alasmar, Diana Avicenna J Med Case Report 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. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4065464/ /pubmed/24982829 http://dx.doi.org/10.4103/2231-0770.133340 Text en Copyright: © Avicenna Journal of Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
El Jabbour, Tony
Aboursheid, Tarek
Keifo, Mohammad Baraa
Maksoud, Ismael
Alasmar, Diana
Kenny-Caffey syndrome type 1
title Kenny-Caffey syndrome type 1
title_full Kenny-Caffey syndrome type 1
title_fullStr Kenny-Caffey syndrome type 1
title_full_unstemmed Kenny-Caffey syndrome type 1
title_short Kenny-Caffey syndrome type 1
title_sort kenny-caffey syndrome type 1
topic Case Report
url 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
work_keys_str_mv AT eljabbourtony kennycaffeysyndrometype1
AT aboursheidtarek kennycaffeysyndrometype1
AT keifomohammadbaraa kennycaffeysyndrometype1
AT maksoudismael kennycaffeysyndrometype1
AT alasmardiana kennycaffeysyndrometype1

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