Skip to main content
Log in

Meckel-Gruber syndrome

  • CASE REPORT
  • Published:
Child's Nervous System Aims and scope Submit manuscript

Abstract

Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 7 September 1996 Revised: 15 January 1997

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gazioğlu, N., Vural, M., Seçkin, M. et al. Meckel-Gruber syndrome. Child's Nerv Syst 14, 142–145 (1998). https://doi.org/10.1007/s003810050198

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s003810050198

Navigation