The gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor gene.

Craniometaphyseal dysplasia (CMD) is an osteochondrodysplasia of unknown etiology characterized by hyperostosis and sclerosis of the craniofacial bones associated with abnormal modeling of the metaphyses. Sclerosis of the skull may lead to asymmetry of the mandible, as well as to cranial nerve compr...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Nürnberg, P, Tinschert, S, Mrug, M, Hampe, J, Müller, C R, Fuhrmann, E, Braun, H S, Reis, A
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 1997
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716005/
https://ncbi.nlm.nih.gov/pubmed/9382103
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