Literature DB >> 15255329

Meckel Gruber syndrome: occurrence in non-consanguineous marriages.

M V C de Silva1, H Senanayake, K D V P Siriwardana.   

Abstract

Meckel Gruber syndrome is an uncommon, lethal, autosomal recessive disorder, associated consistently with polycystic kidneys, posterior encephalocoele and polydactly. We report three cases in non-consanguineous marriages, suggesting that the single gene defect occurs more commonly in non-consanguineous marriages than mutant genes associated with other autosomal recessive disorders that are usually related with consanguineous marriages. The usefulness of prenatal diagnosis is discussed.

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Year:  2004        PMID: 15255329     DOI: 10.4038/cmj.v49i1.3285

Source DB:  PubMed          Journal:  Ceylon Med J        ISSN: 0009-0875


  3 in total

1.  Prenatal diagnosis of Meckel-Gruber syndrome in a pregnancy obtained with ICSI.

Authors:  Claudio Celentano; Federico Prefumo; Marco Liberati; Giuseppina Gallo; Quirino Di Nisio; Sigfried Rotmensch
Journal:  J Assist Reprod Genet       Date:  2006-06-21       Impact factor: 3.412

2.  Meckel Gruber Syndrome: Second trimester diagnosis of a case in a non-consanguineous marriage.

Authors:  Areej Alam; Mehreen Adhi; Raffat Bano; Aisha Zubair; Ammara Mushtaq
Journal:  Pak J Med Sci       Date:  2013-01       Impact factor: 1.088

3.  Meckel-Gruber syndrome: A rare and lethal anomaly with review of literature.

Authors:  Sandesh V Parelkar; Satish P Kapadnis; Beejal V Sanghvi; Prashant B Joshi; Dinesh Mundada; Sanjay N Oak
Journal:  J Pediatr Neurosci       Date:  2013-05
  3 in total

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