Literature DB >> 890111

The Nagar syndrome (acrofacial dysostosis): evidence for autosomal dominant inheritance.

R B Lowry.   

Abstract

A 10-year-old girl with the Nagar acrofacial dysostosis syndrome and normal intelligence is presented. Severe conductive hearing loss remains the major handicap. It is suggested that her syndrome is due to a dominant gene mutation.

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Mesh：

Year:  1977        PMID： 890111

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


  5 in total

1.  Autosomal recessive inheritance of Nager acrofacial dysostosis.

Authors:  J Chemke; B M Mogilner; I Ben-Itzhak; L Zurkowski; D Ophir
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

2.  Synchronous Bilateral Breast Cancer in a Patient With Nager Syndrome.

Authors:  Ryan A Denu; Mark E Burkard
Journal:  Clin Breast Cancer       Date:  2017-01-05       Impact factor: 3.225

Review 3.  Nager acrofacial dysostosis.

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

4.  A.B.R. in Nager type acrofacial dysostosis syndrome.

Authors:  A Mishra; G K Shukla; N Bhatia
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  1999-07

5.  A case report: nager acrofacial dysostosis.

Authors:  Shahin Abdollahi Fakhim; Nikzad Shahidi; Mehrnoush Mousaviagdas
Journal:  Iran J Otorhinolaryngol       Date:  2012
  5 in total

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