Literature DB >> 6711616

Acrofacial dysostosis with severe facial clefting and limb reduction.

E L Kawira, D D Weaver, H A Bender.   

Abstract

We describe two unrelated patients with a severe form of acrofacial dysostosis. Facial defects in both include coloboma of the lids, micrognathia, lateral oral clefting, palatal clefting, and severe auricular anomalies, with one showing bilateral cleft lip and right oblique facial clefting as well. Both have absent forearms and thumbs. Lower limbs were severely reduced in both infants with the feet attached either to the femur or directly to the trunk. Parental consanguinity was present in one case. The condition in these two infants appears to represent either a severe form of Nager acrofacial dysostosis or a new type of acrofacial dysostosis.

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Year:  1984        PMID: 6711616     DOI: 10.1002/ajmg.1320170314

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


  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

Review 2.  Nager acrofacial dysostosis.

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

3.  The Nager acrofacial dysostosis syndrome with the tetralogy of Fallot.

Authors:  E Thompson; R Cadbury; M Baraitser
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

4.  Anaesthetic management of Miller's syndrome.

Authors:  G W Stevenson; S C Hall; B S Bauer; F A Vicari; F L Seleny
Journal:  Can J Anaesth       Date:  1991-11       Impact factor: 5.063

5.  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

  5 in total

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