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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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| Pubblicato in: | BMC Pediatr |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6966812/ https://ncbi.nlm.nih.gov/pubmed/31948427 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-020-1914-8 |
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