Literature DB >> 11008257

Pontocerebellar hypoplasia--how many types?

P G Barth1.   

Abstract

An original article describes a sibship with early fatal pontocerebellar hypoplasia of a yet unclassified type, with the accompanying features of polyhydramnios and neonatal myoclonus. Autopsy in one patient excluded spinal anterior horn involvement, which argues against pontocerebellar hypoplasia type I (PCH-1). The present PCH classification and literature are briefly reviewed. Four previous publications bear similarity to the present report. Definite classification as a genetically separate entity, however, remains elusive pending localization and identification of the gene(s) involved. Copyright 2000 European Paediatric Neurology Society.

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Year:  2000        PMID: 11008257     DOI: 10.1053/ejpn.2000.0294

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  10 in total

Review 1.  Practical approach to prenatal posterior fossa abnormalities using MRI.

Authors:  Laurent Guibaud
Journal:  Pediatr Radiol       Date:  2004-08-04

2.  Pontomedullary disconnection: fetal and neonatal considerations.

Authors:  Emma McCann; David Pilling; Markus Hesseling; Devender Roberts; Nim Subhedar; Elizabeth Sweeney
Journal:  Pediatr Radiol       Date:  2005-04-06

3.  Magnetic resonance imaging of the kinked fetal brain stem: a sign of severe dysgenesis.

Authors:  Annemarie Stroustrup Smith; Deborah Levine; Patrick D Barnes; Richard L Robertson
Journal:  J Ultrasound Med       Date:  2005-12       Impact factor: 2.153

4.  Inherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasia.

Authors:  John C Fyfe; Raba' A Al-Tamimi; Rudy J Castellani; Diana Rosenstein; Daniel Goldowitz; Paula S Henthorn
Journal:  J Comp Neurol       Date:  2010-09-15       Impact factor: 3.215

5.  Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient.

Authors:  Lydie Burglen; Sandra Chantot-Bastaraud; Catherine Garel; Mathieu Milh; Renaud Touraine; Ginevra Zanni; Florence Petit; Alexandra Afenjar; Cyril Goizet; Sabina Barresi; Aurélie Coussement; Christine Ioos; Leila Lazaro; Sylvie Joriot; Isabelle Desguerre; Didier Lacombe; Vincent des Portes; Enrico Bertini; Jean-Pierre Siffroi; Thierry Billette de Villemeur; Diana Rodriguez
Journal:  Orphanet J Rare Dis       Date:  2012-03-27       Impact factor: 4.123

6.  A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings.

Authors:  Zejuan Li; Rhonda Schonberg; Lucia Guidugli; Amy Knight Johnson; Stephen Arnovitz; Sandra Yang; Joseph Scafidi; Marshall L Summar; Gilbert Vezina; Soma Das; Kimberly Chapman; Daniela del Gaudio
Journal:  J Hum Genet       Date:  2015-03-26       Impact factor: 3.172

Review 7.  A developmental and genetic classification for midbrain-hindbrain malformations.

Authors:  A James Barkovich; Kathleen J Millen; William B Dobyns
Journal:  Brain       Date:  2009-12       Impact factor: 13.501

Review 8.  Cerebellar development and disease.

Authors:  Kathleen J Millen; Joseph G Gleeson
Journal:  Curr Opin Neurobiol       Date:  2008-05-29       Impact factor: 6.627

9.  Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Authors:  Yasmin Namavar; Peter G Barth; Paul R Kasher; Fred van Ruissen; Knut Brockmann; Günther Bernert; Karin Writzl; Karen Ventura; Edith Y Cheng; Donna M Ferriero; Lina Basel-Vanagaite; Veerle R C Eggens; Ingeborg Krägeloh-Mann; Linda De Meirleir; Mary King; John M Graham; Arpad von Moers; Nine Knoers; Laszlo Sztriha; Rudolf Korinthenberg; William B Dobyns; Frank Baas; Bwee Tien Poll-The
Journal:  Brain       Date:  2010-10-15       Impact factor: 15.255

10.  A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family.

Authors:  Afrooz Sepahvand; Ehsan Razmara; Fatemeh Bitarafan; Mohammad Galehdari; Ali Reza Tavasoli; Navid Almadani; Masoud Garshasbi
Journal:  Mol Genet Genomic Med       Date:  2020-07-22       Impact factor: 2.183

  10 in total

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