Literature DB >> 3189396

Nager acrofacial dysostosis: evidence for apparent heterogeneity.

D J Goldstein1, L D Mirkin.   

Abstract

Nager acrofacial dysostosis is characterized by malar, mandibular, and maxillary hypoplasia, macrostomia, abnormal ears, and radial defects. The lower limbs are usually normal. Two patients were reported with many of these manifestations, in addition to severe facial clefts and limb deficiency. These more severely affected patients were thought to have a severe form of Nager acrofacial dysostosis or a new syndrome. We report on a patient with limb findings of intermediate severity. This patient also had hydrocephalus, micropolygyria, and tetralogy of Fallot. This may indicate apparent heterogeneity or a single condition with widely variable expression.

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Year:  1988        PMID: 3189396     DOI: 10.1002/ajmg.1320300307

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

Review 1.  Nager acrofacial dysostosis.

Authors:  M T McDonald; J L Gorski
Journal:  J Med Genet       Date:  1993-09       Impact factor: 6.318

2.  Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome.

Authors:  J C Czeschik; C Voigt; Y Alanay; B Albrecht; S Avci; D Fitzpatrick; D R Goudie; U Hehr; A J Hoogeboom; H Kayserili; P O Simsek-Kiper; L Klein-Hitpass; A Kuechler; V López-González; M Martin; S Rahmann; B Schweiger; M Splitt; B Wollnik; H-J Lüdecke; M Zeschnigk; D Wieczorek
Journal:  Hum Genet       Date:  2013-04-09       Impact factor: 4.132

3.  Molecular mechanisms of hearing loss in Nager syndrome.

Authors:  Santosh Kumar Maharana; Jean-Pierre Saint-Jeannet
Journal:  Dev Biol       Date:  2021-04-14       Impact factor: 3.148

  3 in total

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