Literature DB >> 12044856

Meckel Gruber syndrome: a first trimester diagnosis of a recurrent case.

Hamit Alper Tanriverdi1, Hans Joachim Hendrik, Kubilay Ertan, Werner Schmidt.   

Abstract

We report of a case of Meckel Gruber Syndrome (MGS) in a woman, who suffered previously from a pregnancy with the same disorder. MGS, consisting of an occipital encephalocele, bilateral cystic kidneys and postaxial polydactyly, is a rare autosomal recessive disorder, with a recurrence risk of 25%. With the present technology, a targeted ultrasound in the late embryonic or early fetal stages of pregnancy has the potential to diagnose this syndrome. Clinical screening in further pregnancies is of utmost importance and the management of such cases is presented.

Entities:  

Mesh:

Year:  2002        PMID: 12044856     DOI: 10.1016/s0929-8266(02)00009-5

Source DB:  PubMed          Journal:  Eur J Ultrasound        ISSN: 0929-8266


  2 in total

1.  [Meckel Gruber syndrome: about a rare case].

Authors:  Sanaa Itchimouh; Karima Khabtou; Sakher Mahdaoui; Houssine Boufettal; Naima Samouh
Journal:  Pan Afr Med J       Date:  2016-09-29

2.  DDA: A Novel Network-Based Scoring Method to Identify Disease-Disease Associations.

Authors:  Apichat Suratanee; Kitiporn Plaimas
Journal:  Bioinform Biol Insights       Date:  2015-12-08
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.