Literature DB >> 1248161

Aarskog syndrome: new oral-facial findings.

M Melnick, E D Shields.   

Abstract

The Aarskog syndrome is characterized by short stature with typical facial, digital and genital anomalies. A further case is reported which presented with the uncommon finding of ophthalmoplegia and three previously unreported oral-facial findings: enamel dysplasia, a "col" deformity of the anterior mandible and a paresis of the facial muscles innervated by the VII cranial nerve. The implications of genetic heterogeneity in this nosologic classification are discussed.

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Year:  1976        PMID: 1248161     DOI: 10.1111/j.1399-0004.1976.tb01545.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  4 in total

1.  Aarskog syndrome.

Authors:  M E Porteous; D R Goudie
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

2.  The Aarskog syndrome.

Authors:  J P Fryns; J Macken; L Vinken; L Igodt-Ameye; H van den Berghe
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

3.  Intelligence and development in Aarskog syndrome.

Authors:  L J Logie; M E Porteous
Journal:  Arch Dis Child       Date:  1998-10       Impact factor: 3.791

4.  Cerebrovascular disease associated with Aarskog-Scott syndrome.

Authors:  Michael L Diluna; Nduka M Amankulor; Michele H Johnson; Murat Gunel
Journal:  Neuroradiology       Date:  2007-02-10       Impact factor: 2.995

  4 in total

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