Atypical presentation of Prader-Willi syndrome with Klinefelter (XXY karytype) and craniosynostosis Síndrome de Prader-Willi em paciente com Klinefelter (cariótipo XXY) e craniossinostose

Prader-Willi syndrome is a mental retardation genetic disorder also characterized by hypogonadism, hyperphagia and obesity. We report on a four-years-old boy, born to consanguineous parents, with uncommon co-occurrence of Prader-Willi syndrome, 47,XXY karyotype (Klinefelter syndrome) and coronal cra...

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Egile Nagusiak:	Daniel R. Carvalho, Clovis S. Trad, João M. Pina-Neto
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Thieme Revinter Publicações 2006-06-01
Saila:	Arquivos de Neuro-Psiquiatria
Gaiak:	cariótipo XXY síndrome de Prader-Willi síndrome de Klinefelter craniossinostose XXY karyotype Prader-Willi syndrome Klinefelter syndrome craniosynostosis
Sarrera elektronikoa:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000200024
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