Literature DB >> 10589063

Autosomal recessive hydrocephalus due to congenital stenosis of the aqueduct of sylvius.

H Hamada1, H Watanabe, M Sugimoto, M Yasuoka, N Yamada, T Kubo.   

Abstract

Isolated hydrocephalus due to congenital stenosis of the aqueduct of Sylvius is almost always an X-linked recessive inherited condition. We describe a brother and sister with isolated hydrocephalus from congenital aqueductal stenosis. We believe that these two occurrences represent a rare autosomal recessive form of this abnormality. In assessing a first known occurrence of hydrocephalus with stenosis of the aqueduct of Sylvius in a family, the rare possibility of autosomal inheritance must be considered in genetic counselling.

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Year:  1999        PMID: 10589063

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  6 in total

1.  Disruption of the mouse Jhy gene causes abnormal ciliary microtubule patterning and juvenile hydrocephalus.

Authors:  Oliver K Appelbe; Bryan Bollman; Ali Attarwala; Lindy A Triebes; Hilmarie Muniz-Talavera; Daniel J Curry; Jennifer V Schmidt
Journal:  Dev Biol       Date:  2013-07-29       Impact factor: 3.582

2.  Ventricular dilatations.

Authors:  Catherine Garel; Dominique Luton; Jean-François Oury; Pierre Gressens
Journal:  Childs Nerv Syst       Date:  2003-07-16       Impact factor: 1.475

Review 3.  Genetics of human hydrocephalus.

Authors:  Jun Zhang; Michael A Williams; Daniele Rigamonti
Journal:  J Neurol       Date:  2006-06-13       Impact factor: 4.849

4.  Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus.

Authors:  Nesreen K Al-Jezawi; Aisha M Al-Shamsi; Jehan Suleiman; Salma Ben-Salem; Anne John; Ranjit Vijayan; Bassam R Ali; Lihadh Al-Gazali
Journal:  BMC Med Genet       Date:  2018-03-02       Impact factor: 2.103

5.  Idiopathic Aqueductal Stenosis: Late Neurocognitive Outcome in ETV Operated Adult Patients.

Authors:  Matteo Martinoni; Giovanni Miccoli; Luca Albini Riccioli; Francesca Santoro; Giacomo Bertolini; Corrado Zenesini; Diego Mazzatenta; Alfredo Conti; Luigi Maria Cavallo; Giorgio Palandri
Journal:  Front Neurol       Date:  2022-04-07       Impact factor: 4.003

6.  L1CAM mutation in association with X-linked hydrocephalus and Hirschsprung's disease.

Authors:  Sha-Ron Jackson; Yigit S Guner; Russell Woo; Linda M Randolph; Henri Ford; Cathy E Shin
Journal:  Pediatr Surg Int       Date:  2009-07-30       Impact factor: 1.827

  6 in total

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