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.
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/39
English
Autism; Comorbidity; Development; Greig cephalopolysyndactyly syndrome; Intellectual disability; Neuropsychological phenotype; Acrocephalosyndactylia; Adult; Autism Spectrum Disorder; Behavior Therapy; Child; Chromosome Deletion; Genetic Linkage; Humans; Male; Nerve Tissue Proteins; Neuropsychological Tests; Phenotype; Zinc Finger Protein Gli3
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].
Siracusano, M; Riccioni, A; Baratta, A; Baldi, M; Curatolo, P; Mazzone, L
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
Siracusano_et_al Greig Syndrome.pdf

accesso aperto

Licenza: Copyright dell'editore
Dimensione 848.09 kB
Formato Adobe PDF
848.09 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/245204
Citazioni
  • ???jsp.display-item.citation.pmc??? 2
  • Scopus 5
  • ???jsp.display-item.citation.isi??? ND
social impact