Literature DB >> 8736156

[Pyle's syndrome: report of a case].

C Oppenheimer1, B C Oliveira, M Sogabe, W Sanvito.   

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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Year:  1996        PMID: 8736156     DOI: 10.1590/s0004-282x1996000100020

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  1 in total

1.  Pyle disease (metaphyseal dysplasia) presenting in two adult sisters.

Authors:  Diego Ximenes Soares; Amália Mapurunga Almeida; André Rodrigues Façanha Barreto; Ilze Jucá Alencar E Silva; José Daniel Vieira de Castro; Francisco José Magalhães Pinto; Daniel Aguiar Dias; Lindenberg Barbosa Aguiar
Journal:  Radiol Case Rep       Date:  2016-11-01
  1 in total

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