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Article

Meckel Gruber syndrome, A case report.

Organogenesis - 1 Jan 2015

Aslan Kiper, Külahçı Aslan Elif, Orhan Adnan, Atalay Mehmet Aral

Abstract excerpt

INTRODUCTION: Meckel-Gruber Syndrome was first described by J R Meckel in 1822. It is an autosomal recessive disorder, and is caused by the failure of mesodermal induction. The typical triad of Meckel-Gruber Syndrome (MGS) involves meningo-encephalocele, polycystic kidneys and postaxial polydactyly. The worldwide incidence varies from 1 in 1.300 to 1 in 140.000 live births. CASE: In this report, we present a case...

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Identifiers

PMID: 26037304
DOI: 10.1080/15476278.2015.1055431
PMCID: PMC4594365

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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