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 developmental features of this syndrome.
Siracusano, M., Riccioni, A., Baratta, A., Baldi, M., Curatolo, P., Mazzone, L. (2019). Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report. JOURNAL OF MEDICAL CASE REPORTS, 13(1), 100 [10.1186/s13256-019-2043-6].
Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report
Siracusano M.
;Baldi M.;Mazzone L.
2019-01-01
Abstract
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 developmental features of this syndrome.File in questo prodotto:
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