Your browser doesn't support javascript.
loading
[Pyle's syndrome: report of a case]. / Síndrome de Pyle: relato de caso.
Oppenheimer, C; Oliveira, B C; Sogabe, M; Sanvito, W.
Affiliation
  • Oppenheimer C; Disciplina de Neurologia da Faculdade de Ciências Médicas, São Paulo, Brasil.
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.
Subject(s)
Search on Google
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
Search on Google
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