Cleidocranial dysplasia with growth hormone deficiency: a case report

BACKGROUND: Cleidocranial dysplasia (CCD) is a rare skeletal disorder with autosomal dominant inheritance that is characterized by hypoplastic clavicles, delayed closure of the cranial sutures, dental abnormalities, and short stature, among other features. The responsible gene for CCD is RUNX2 locat...

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Detalles Bibliográficos
Autores principales: Takaki, Nozomi, Mori, Jun, Matsuo, Satoshi, Osamura, Toshio, Michigami, Toshimi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966812/
https://www.ncbi.nlm.nih.gov/pubmed/31948427
http://dx.doi.org/10.1186/s12887-020-1914-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966812/
https://www.ncbi.nlm.nih.gov/pubmed/31948427
http://dx.doi.org/10.1186/s12887-020-1914-8

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