[Pyle's syndrome: report of a case]. / Síndrome de Pyle: relato de caso.
Arq Neuropsiquiatr
; 54(1): 120-3, 1996 Mar.
Article
in Pt
| MEDLINE
| ID: mdl-8736156
ABSTRACT
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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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Osteochondrodysplasias
Type of study:
Diagnostic_studies
/
Etiology_studies
Limits:
Adolescent
/
Female
/
Humans
Language:
Pt
Journal:
Arq Neuropsiquiatr
Year:
1996
Document type:
Article
Affiliation country:
Brazil