A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment

Cleidocranial dysplasia (CCD) is a rare congenital autosomal dominant skeletal disorder that is characterized by hypoplasia or aplasia of clavicles, failure of cranial suture closure, dental anomalies, short stature and other changes in skeletal patterning and growth. The gene responsible for pathog...

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Detalles Bibliográficos
Autores principales: Çamtosun, Emine, Akıncı, Ayşehan, Demiral, Emine, Tekedereli, İbrahim, Sığırcı, Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745455/
https://www.ncbi.nlm.nih.gov/pubmed/30468148
http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0211

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745455/
https://www.ncbi.nlm.nih.gov/pubmed/30468148
http://dx.doi.org/10.4274/jcrpe.galenos.2018.2018.0211

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