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Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report
BACKGROUND: Greig cephalopolysyndactyly syndrome is a rare multiple congenital anomaly syndrome characterized by the triad of polysyndactyly (preaxial or mixed preaxial and postaxial), macrocephaly, and ocular hypertelorism. Little is known about the neuropsychological phenotype and the developmenta...
Enregistré dans:
| Publié dans: | J Med Case Rep |
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| Auteurs principaux: | , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
BioMed Central
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6477736/ https://ncbi.nlm.nih.gov/pubmed/31010437 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-019-2043-6 |
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