Literature DB >> 2748737

A significant feature of Nager's syndrome: palatal agenesis.

I T Jackson1, B Bauer, J Saleh, C Sullivan, L C Argenta.   

Abstract

Nager's syndrome, which has the facial features of Treacher Collins syndrome, preaxial upper limb defects, short stature, and frequently subnormal intelligence, is very rare. Five new cases have been collected. In four, there was virtually total absence of the soft palate. This has been described in two patients in the past. Differing methods of correcting this are presented.

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Year:  1989        PMID: 2748737     DOI: 10.1097/00006534-198908000-00005

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  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.  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

3.  A case report: nager acrofacial dysostosis.

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

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