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...

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Detalles Bibliográficos
Autores principales: Siracusano, Martina, Riccioni, Assia, Baratta, Antonia, Baldi, Maurizia, Curatolo, Paolo, Mazzone, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477736/
https://www.ncbi.nlm.nih.gov/pubmed/31010437
http://dx.doi.org/10.1186/s13256-019-2043-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477736/
https://www.ncbi.nlm.nih.gov/pubmed/31010437
http://dx.doi.org/10.1186/s13256-019-2043-6

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