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The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly
PURPOSE: Greig cephalopolysyndactyly (GCPS) (OMIM 175700), a rare autosomal dominant disorder, is characterized by a distinct combination of craniofacial, hand and foot malformations. The hand and foot malformations often require orthopedic assessment and treatment. The disorder is caused by point m...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2656707/ https://ncbi.nlm.nih.gov/pubmed/19308487 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11832-007-0022-8 |
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