Literature DB >> 15551328

Familial lipomyelomeningocele: a further report.

Peter Kannu1, Christopher Furneaux, Salim Aftimos.   

Abstract

Lipomyelomeningocele is a form of spina bifida occulta with a distinct pathogenesis that differentiates it from open neural tube defects. Familial forms are rare and the condition may be polygenic. We report on 2 affected siblings with similar lesions and raise the possibility of an autosomal recessive pattern of inheritance with implications for genetic counselling. (c) 2004 Wiley-Liss, Inc.

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Year:  2005        PMID: 15551328     DOI: 10.1002/ajmg.a.30404

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  3 in total

1.  Gender and morphogenetic variability of patients with spina bifida occulta and spina bifida aperta: prospective population-genetic study.

Authors:  D Nikolic; I Petronic; S Cvjeticanin; R Brdar; D Cirovic; M Bizic; L Konstantinovic; D Matanovic
Journal:  Hippokratia       Date:  2012-01       Impact factor: 0.471

Review 2.  Surgical management of lipomyelomeningocele in children: Challenges and considerations.

Authors:  Kathryn M Wagner; Jeffrey S Raskin; Daniel Hansen; Gaddum D Reddy; Andrew Jea; Sandi Lam
Journal:  Surg Neurol Int       Date:  2017-04-26

3.  Lateral lower thoracic lipomyelomeningocele: a case report.

Authors:  Fatih Serhat Erol; Necati Ucler; Huseyin Yakar
Journal:  Cases J       Date:  2009-07-01
  3 in total

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