Literature DB >> 3510965

MURCS association with additional congenital anomalies.

R A Greene, M J Bloch, D S Huff, R V Iozzo.   

Abstract

The postmortem findings in a patient with the MURCS association (müllerian duct aplasia/hypoplasia, renal agenesis or ectopy, and cervicothoracic somite dysplasia) are reported. This is the first autopsy study since the syndrome was recognized. The autopsy revealed abnormalities of the venous, pulmonary, and central nervous systems that had not been reported previously in patients with this syndrome. A review of the literature suggested that although the MURCS association usually occurs sporadically, as in this case, a familial association is occasionally present. In some cases the MURCS association may be a genetically determined pleiotropic condition.

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Year:  1986        PMID: 3510965     DOI: 10.1016/s0046-8177(86)80160-5

Source DB:  PubMed          Journal:  Hum Pathol        ISSN: 0046-8177            Impact factor:   3.466


  3 in total

1.  MURCS in a male?

Authors:  D G Wellesley; S F Slaney
Journal:  J Med Genet       Date:  1995-04       Impact factor: 6.318

2.  MURCS association: case report and review.

Authors:  C Braun-Quentin; C Billes; B Böwing; D Kotzot
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

3.  Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association).

Authors:  Gerda Hofstetter; Nicole Concin; Christian Marth; Tuula Rinne; Martin Erdel; Andreas Janecke
Journal:  Wien Klin Wochenschr       Date:  2008       Impact factor: 1.704

  3 in total

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