[Pyle's syndrome: report of a case]. / Síndrome de Pyle: relato de caso.
Arq Neuropsiquiatr
; 54(1): 120-3, 1996 Mar.
Article
em Pt
| MEDLINE
| ID: mdl-8736156
Pyle's syndrome is a rare picture of osseous dysplasia with autosomal recessive inheritance beginning in early childhood. The authors report the case of a 15-years-old female patient with bilateral lower motor neuron facial palsy, progressive hearing loss, salience of frontal bone, metaphyseal enlargement of the lower limbs and genu valgus. In the present paper we briefly review the clinical features and the differential diagnosis of Pyle's syndrome.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Osteocondrodisplasias
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
Limite:
Adolescent
/
Female
/
Humans
Idioma:
Pt
Revista:
Arq Neuropsiquiatr
Ano de publicação:
1996
Tipo de documento:
Article
País de afiliação:
Brasil
País de publicação:
Alemanha