Literature DB >> 8369884

A severe case of Beare-Stevenson syndrome and associated congenital deformities.

J M Andrews1, D M Martins, R R Ramos, L M Ferreira.   

Abstract

A severe case of congenital anomalies is described, with several characteristics of Beare-Stevenson syndrome, such as cutis gyrata, acanthosis nigricans, craniofacial anomalies, ear defects, enlarged umbilical stump and anogenital anomalies. He does not have craniosynostosis or clover leaf skull, which has also been described in this syndrome. This patient also shows hands and feet anomalies, absence of skin adnexa in several locations and dental anomalies, which could suggest an associated ectodermal dysplasia.

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Year:  1993        PMID: 8369884     DOI: 10.1016/0007-1226(93)90053-e

Source DB:  PubMed          Journal:  Br J Plast Surg        ISSN: 0007-1226


  1 in total

1.  Report of a Father With Congenital Bilateral Absence of the Vas Deferens Fathering a Child With Beare-Stevenson Syndrome.

Authors:  Leonardo C Ferreira; José H Dantas Junior
Journal:  Front Genet       Date:  2020-02-25       Impact factor: 4.599

  1 in total

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