Literature DB >> 15672385

Cerebellar hypoplasia-endosteal sclerosis: a long term follow-up.

Heval M Ozgen1, Wouterina C G Overweg-Plandsoen, Janneke Blees-Pelk, Philip P Besselaar, Raoul C M Hennekam.   

Abstract

Cerebellar hypoplasia with endosteal sclerosis is an infrequent entity that has been described in only four cases. Major clinical symptoms are cerebellar hypoplasia causing ataxia, hypotonia, mild to moderate developmental delay, microcephaly, growth retardation, endosteal sclerosis, tooth eruption disturbances, and hip dislocations. We report on a girl with this entity, whom we followed for 11 years. The endosteal sclerosis remained stationary over time, as were the clinical neurological symptoms, but neuroadiological symptoms were slowly progressive. We provide a short review of this probably autosomal recessively inherited disorder. (c) 2005 Wiley-Liss, Inc. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15672385     DOI: 10.1002/ajmg.a.30589

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


  2 in total

1.  Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.

Authors:  Nicole I Wolf; Adeline Vanderver; Rosalina M L van Spaendonk; Raphael Schiffmann; Bernard Brais; Marianna Bugiani; Erik Sistermans; Coriene Catsman-Berrevoets; Johan M Kros; Pedro Soares Pinto; Daniela Pohl; Sandya Tirupathi; Petter Strømme; Ton de Grauw; Sébastien Fribourg; Michelle Demos; Amy Pizzino; Sakkubai Naidu; Kether Guerrero; Marjo S van der Knaap; Geneviève Bernard
Journal:  Neurology       Date:  2014-10-22       Impact factor: 9.910

2.  Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder.

Authors:  Jamal Ghoumid; Florence Petit; Odile Boute-Benejean; Frédéric Frenois; Maryse Cartigny; Clémence Vanlerberghe; Thomas Smol; Roseline Caumes; Nicolas de Roux; Sylvie Manouvrier-Hanu
Journal:  Eur J Hum Genet       Date:  2017-06-07       Impact factor: 4.246

  2 in total

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