Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a rare cause of parainfectious rhabdomyolysis.
Eur J Pediatr
; 166(7): 747-9, 2007 Jul.
Article
em En
| MEDLINE
| ID: mdl-17195938
ABSTRACT
Congenital cataracts-facial dysmorphism-neuropathy syndrome (CCFDN, MIM 604168), is a recently delineated neurogenetic disease causing recurrent episodes of rhabdomyolysis; prevention and early diagnosis of rhabdomyolysis should be part of the clinical management of the disease.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Rabdomiólise
/
Catarata
/
Doenças do Nervo Facial
Tipo de estudo:
Screening_studies
Limite:
Child, preschool
/
Humans
/
Male
Idioma:
En
Revista:
Eur J Pediatr
Ano de publicação:
2007
Tipo de documento:
Article
País de afiliação:
Grécia