Literature DB >> 25293531

Langer-Giedion syndrome associated with congenital dural arterio-venous fistula.

Severina Leu1, Anton Valavanis, Gerasimos Baltsavias.   

Abstract

Langer-Giedion syndrome (LGS) is a rare disease caused by deletion of chromosome 8q23.3-q24.11. Clinical manifestations include among others multiple exostoses, short stature, intellectual disability, and typical facial dysmorphism. Dural arterio-venous shunts (DAVS) in the pediatric age are rare lesions, which have been classified into three types: dural sinus malformations (DSM), infantile type DAVS (IDAVS), and adult type DAVS (ADAVS). We report a case of a patient with a known LGS who was diagnosed with complex intracranial dural AV fistula at the age of 20. An association between LGS and intracranial dural AV fistulas has to our knowledge never been reported before.

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Year:  2014        PMID: 25293531     DOI: 10.1007/s00381-014-2570-9

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


  7 in total

1.  The widened spectrum of multiple cartilaginous exostosis (MCE).

Authors:  A Giedion; R Kesztler; F Muggiasca
Journal:  Pediatr Radiol       Date:  1975-03-20

2.  Dural Sinus Malformations (DSM) with Giant Lakes, in Neonates and Infants. Review of 30 Consecutive Cases.

Authors:  M Barbosa; J Mahadevan; Y C Weon; Y Yoshida; A Ozanne; G Rodesch; H Alvarez; P Lasjaunias
Journal:  Interv Neuroradiol       Date:  2004-10-22       Impact factor: 1.610

Review 3.  Complex chromosomal rearrangements causing Langer-Giedion syndrome atypical phenotype: genotype-phenotype correlation and literature review.

Authors:  Gerarda Cappuccio; Rita Genesio; Valentina Ronga; Alberto Casertano; Antonella Izzo; Maria Pia Riccio; Carmela Bravaccio; Maria Carolina Salerno; Lucio Nitsch; Generoso Andria; Daniela Melis
Journal:  Am J Med Genet A       Date:  2013-12-19       Impact factor: 2.802

4.  Anatomoclinical Aspects of Dural Arteriovenous Shunts in Children. Review of 29 cases.

Authors:  P Lasjaunias; G Magufis; A Goulao; R Piske; S Suthipongchai; R Rodesch; H Alvarez
Journal:  Interv Neuroradiol       Date:  2001-05-15       Impact factor: 1.610

5.  Microcephaly-thin corpus callosum syndrome maps to 8q23.2-q24.12.

Authors:  Ayelet Halevy; Lina Basel-Vanagaite; Avinoam Shuper; Shlomit Helman; Adi Har-Zahav; Efrat Birk; Idit Maya; Liora Kornreich; Dov Inbar; Gudrun Nürnberg; Peter Nürnberg; Tamar Steinberg; Rachel Straussberg
Journal:  Pediatr Neurol       Date:  2012-06       Impact factor: 3.372

6.  Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion.

Authors:  Wim Wuyts; Dominique Roland; Hermann-Josef Lüdecke; Jan Wauters; Martine Foulon; Wim Van Hul; Lionel Van Maldergem
Journal:  Am J Med Genet       Date:  2002-12-15

7.  The tricho-rhino-phalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature.

Authors:  L O Langer; N Krassikoff; R Laxova; M Scheer-Williams; L D Lutter; R J Gorlin; C G Jennings; D W Day
Journal:  Am J Med Genet       Date:  1984-09
  7 in total

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