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...

全面介紹

書目詳細資料

Principais autores:	Daniel R. Carvalho, Clovis S. Trad, João M. Pina-Neto
格式:	Artigo
語言:	Inglês
出版:	Thieme Revinter Publicações 2006-06-01
叢編:	Arquivos de Neuro-Psiquiatria
主題:	cariótipo XXY síndrome de Prader-Willi síndrome de Klinefelter craniossinostose XXY karyotype Prader-Willi syndrome Klinefelter syndrome craniosynostosis
在線閱讀:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000200024
標簽:	添加標簽 沒有標簽, 成為第一個標記此記錄!