Distal arthrogryposis and neonatal hypotonia: an unusual presentation of Prader-Willi syndrome (PWS).
J Perinatol
; 24(11): 733-4, 2004 Nov.
Article
em En
| MEDLINE
| ID: mdl-15510104
ABSTRACT
The clinical features of Prader-Willi Syndrome (PWS) in the neonate are marked by hypotonia, absence of crying, and feeding difficulties, but the clinical nature of PWS in utero remains unclear. We report a case of PWS with fetal immobility and distal arthrogryposis in a girl admitted the first day of life to the neonatal intensive care unit for severe hypotonia and respiratory distress.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Síndrome de Prader-Willi
/
Artrogripose
/
Hipotonia Muscular
Limite:
Female
/
Humans
/
Newborn
Idioma:
En
Ano de publicação:
2004
Tipo de documento:
Article