Meckel Gruber Syndrome- A Case Report And Review of Literature

Authors

  • Sümeyra Nergiz Department of Gynecology and Obstetrics Adnan Menderes University School of Medicine, Aydın
  • Selda Demircan Sezer Department of Gynecology and Obstetrics Adnan Menderes University School of Medicine, Aydın
  • Sündüz Özlem Altınkaya Department of Gynecology and Obstetrics Adnan Menderes University School of Medicine, Aydın
  • Mert Küçük Department of Gynecology and Obstetrics Adnan Menderes University School of Medicine, Aydın
  • Hasan Yüksel Department of Gynecology and Obstetrics Adnan Menderes University School of Medicine, Aydın

Keywords:

Meckel gruber syndrome, Ultrasonography, Prenatal diagnosis

Abstract

Meckel-Gruber syndrome (MGS) is a lethal autosomal recessive disorder. MGS is thought to be caused by ciliary dysfunction. The worldwide incidence of MGS varies from 1 in 13 250 to 1 in 140.000 live births. MGS is characterized by three main symptoms: central nervous system (CNS) malformations, tetramelic postaxial polydactyly and cystic renal dysplasia with associated fibrocystic changes of the liver, pancreas and epididymis. Here a case of MG syndrome, diagnosed in early weeks of gestation was reported.

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Published

2014-12-30

How to Cite

1.
Nergiz S, Demircan Sezer S, Altınkaya S Özlem, Küçük M, Yüksel H. Meckel Gruber Syndrome- A Case Report And Review of Literature. Gynecol Obstet Reprod Med [Internet]. 2014Dec.30 [cited 2024Apr.19];20(3):175-7. Available from: https://www.gorm.com.tr/index.php/GORM/article/view/169

Issue

Vol. 20 No. 3 (2014)

Section

Case Reports

License

Copyright (c) 2014 Sümeyra Nergiz, Selda Demircan Sezer, Sündüz Özlem Altınkaya, Mert Küçük, Hasan Yüksel

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

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