Literature DB >> 2816994

VACTERL with hydrocephalus: further delineation of the syndrome(s)

J A Evans1, L C Stranc, P Kaplan, A G Hunter.   

Abstract

Central nervous system defects including hydrocephalus are rare in cases of VACTERL association. However, recent reports suggest that there may be one or more disorders in which this combination of anomalies occurs. We report 8 additional patients including a recurrence in a previously described family, review the literature, and provide some population-based data of VACTERL-type anomalies in hydrocephalus cases. VACTERL with hydrocephalus appears distinct from hydrolethalus and similar conditions but is itself heterogeneous. The pattern of inheritance of the disorders involved is unclear, but autosomal recessive and sex-linked forms likely occur. The prognosis of VACTERL cases with hydrocephalus appears much poorer than for those with classic VACTERL anomalies, and the recurrence risk may be higher than for either the VACTERL association or isolated hydrocephalus.

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Year:  1989        PMID: 2816994     DOI: 10.1002/ajmg.1320340209

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Tracheo-oesophageal fistula with hydrocephalus.

Authors:  S Budhiraja; K N Rattan; S Gupta; S K Pandit
Journal:  Indian J Pediatr       Date:  1997 Sep-Oct       Impact factor: 1.967

Review 2.  Townes-Brocks syndrome.

Authors:  C M Powell; R C Michaelis
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

3.  VACTERL plus hydrocephalus: a monogenic lethal condition.

Authors:  J Kunze; S Huber-Schumacher; M Vogel
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

4.  Considering the Embryopathogenesis of VACTERL Association.

Authors:  R E Stevenson; A G W Hunter
Journal:  Mol Syndromol       Date:  2013-02

5.  VACTERL-H syndrome: first trimester diagnosis.

Authors:  Banu Dane; Zeynep Kayaoğlu; Cem Dane; Figen Aksoy
Journal:  J Turk Ger Gynecol Assoc       Date:  2011-12-01

6.  Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome.

Authors:  S T Holden; J J Cox; I Kesterton; N S Thomas; C Carr; C G Woods
Journal:  J Med Genet       Date:  2006-05-05       Impact factor: 6.318

7.  Beyond Gómez-López-Hernández syndrome: recurring phenotypic themes in rhombencephalosynapsis.

Authors:  Hannah M Tully; Jennifer C Dempsey; Gisele E Ishak; Margaret P Adam; Cynthia J R Curry; Pedro Sanchez-Lara; Alasdair Hunter; Karen W Gripp; Judith Allanson; Christopher Cunniff; Ian Glass; Kathleen J Millen; Daniel Doherty; William B Dobyns
Journal:  Am J Med Genet A       Date:  2012-09-10       Impact factor: 2.802

8.  Crossed nonfused renal ectopia with variant blood vessels: a rare congenital renal anomaly.

Authors:  Nawal Ebrahim Al-Hamar; Khalid Khan
Journal:  Radiol Case Rep       Date:  2016-11-29
  8 in total

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