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A rare case of cleidocranial dysplasia presenting with failure to thrive
Cleidocranial dysplasia (CCD) is a rare (1:1,000,000) congenital condition secondary to spontaneous mutation (40%) or autosomal dominant inheritance (60%) affecting skeletal and dental systems. Hypomineralization of the hypoplastic clavicles and/or cranium is the major feature observed by prenatal u...
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| Publicado no: | J Nat Sci Biol Med |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4367046/ https://ncbi.nlm.nih.gov/pubmed/25810671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-9668.149198 |
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