Literature DB >> 421363

Familial occurrence of syngnathia congenita syndrome.

I Gassner, W Müller, H Rössler, J Kofler, G Mitterstieler.   

Abstract

A case of familial occurrence of syngnathia congenita in mother and child is described; this syndrome has been seen only sporadically until now. Due to the distinct appearance of the intraoral chords--they were situated on both sides between the ridges of the jaw and also between the left half of the bifid uvula and the retrolingual region--a relationship to the autosomal-dominantly transmitted Cleft Palate Lateral Synechiae Syndrome (CPLS-Syndrome) is suspected. Complete penetrance with different expressivity may explain the different clinical manifestations of the cases seen up to now and the absence of bifid uvula in the mother of our patient. The probable pathogenesis during embryological development is discussed.

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Year:  1979        PMID: 421363     DOI: 10.1111/j.1399-0004.1979.tb00974.x

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


  4 in total

1.  Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32.

Authors:  M M Lees; R M Winter; S Malcolm; H M Saal; L Chitty
Journal:  J Med Genet       Date:  1999-12       Impact factor: 6.318

2.  Popliteal pterygium syndrome.

Authors:  U G Froster-Iskenius
Journal:  J Med Genet       Date:  1990-05       Impact factor: 6.318

3.  Congenital Maxillomandibular Syngnathia: Review of Literature and Proposed New Classification System.

Authors:  Vijay Kumar; Vidya Rattan; Sachin Rai
Journal:  J Maxillofac Oral Surg       Date:  2019-11-20

4.  Popliteal pterygium syndrome: A rare syndrome.

Authors:  Surya Rao Rao Venkata Mahipathy; Alagar Raja Durairaj; Narayanamurthy Sundaramurthy; Manimaran Ramachandran
Journal:  Indian J Plast Surg       Date:  2018 May-Aug
  4 in total

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