Literature DB >> 671493

Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs.

P Jackson, H G Kohler.   

Abstract

A Pakistani couple, who were first cousins once removed through their fathers, and whose mothers were also related, had two liveborn children, a boy and a girl. Both children died within 2 hours of birth with occipital encephalocele, microcephaly, polycystic kidneys, and cystic distension of intrahepatic bile ducts. Both children had normal karyotypes. These abnormalities constitute Meckel's syndrome (dysencephalia splanchno-cystica); this is the fifth report of parental consanguinity, adding further support to the evidence for autosomal recessive inheritance of the disorder.

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Year:  1978        PMID: 671493      PMCID: PMC1013688          DOI: 10.1136/jmg.15.3.242

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  5 in total

1.  Comments upon the classification of infantile polycystic diseases of the liver and kidney, based upon three-dimensional reconstruction of the liver.

Authors:  C M Adams; D M Danks; P E Campbell
Journal:  J Med Genet       Date:  1974-09       Impact factor: 6.318

2.  [Familial polydactyly with neuro-cranial dysplasia].

Authors:  R Walbaum; P Dehaene; F Duthoit
Journal:  Ann Genet       Date:  1967-03

3.  Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies.

Authors:  C C Tucker; S C Finley; E S Tucker; W H Finley
Journal:  J Med Genet       Date:  1966-06       Impact factor: 6.318

4.  Genetics of the Meckel syndrome (dysencephalia splanchnocystica).

Authors:  Y E Hsia; M Bratu; A Herbordt
Journal:  Pediatrics       Date:  1971-08       Impact factor: 7.124

5.  Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.

Authors:  K Fried; E Liban; M Lurie; S Friedman; S H Reisner
Journal:  J Med Genet       Date:  1971-09       Impact factor: 6.318

  5 in total
  4 in total

1.  The Meckel Syndrome. Pathological and cytogenetic observations in eight cases.

Authors:  P Moerman; E Verbeken; J P Fryns; P Goddeeris; J M Lauweryns
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  Are bowing of long tubular bones and preaxial polydactyly signs of the Meckel syndrome?

Authors:  F Majewski; H Stöss; T Goecke; H Kemperdick
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  High incidence of Meckel's syndrome in Gujarati Indians.

Authors:  I D Young; A B Rickett; M Clarke
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

4.  Meckel-Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe.

Authors:  Ingeborg Barisic; Ljubica Boban; Maria Loane; Ester Garne; Diana Wellesley; Elisa Calzolari; Helen Dolk; Marie-Claude Addor; Jorieke Eh Bergman; Paula Braz; Elizabeth S Draper; Martin Haeusler; Babak Khoshnood; Kari Klungsoyr; Anna Pierini; Annette Queisser-Luft; Judith Rankin; Anke Rissmann; Christine Verellen-Dumoulin
Journal:  Eur J Hum Genet       Date:  2014-09-03       Impact factor: 4.246

  4 in total

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