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A three-year clinical investigation of a Chinese child with craniometaphyseal dysplasia caused by a mutated ANKH gene
BACKGROUND: Craniometaphyseal dysplasia (CMD) is a rare genetic disorder. Autosomal dominant CMD (AD-CMD) is caused by mutations in the ANKH gene. Affected individuals typically have distinctive facial features including progressive thickening of the craniofacial bones. Treatment for AD-CMD primaril...
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| Publicado no: | World J Clin Cases |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7953411/ https://ncbi.nlm.nih.gov/pubmed/33748234 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12998/wjcc.v9.i8.1853 |
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