Literature DB >> 1776639

Autosomal recessive cerebellar hypoplasia and endosteal sclerosis: a newly recognized syndrome.

J Charrow1, A K Poznanski, F M Unger, M Robinow.   

Abstract

We describe a brother and sister and an unrelated boy with congenital cerebellar hypoplasia and endosteal sclerosis. All 3 children presented with ataxia and developmental delay, and were found to have microcephaly, short stature, oligodontia, strabismus, nystagmus, and congenital hip dislocation. A previously published case is reviewed. The disorder appears to represent a newly recognized autosomal recessive syndrome.

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Year:  1991        PMID: 1776639     DOI: 10.1002/ajmg.1320410417

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


  4 in total

1.  Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: "D-CHRAMPS syndrome".

Authors:  Dana Hiyasat; Munir A Dehyyat; Saleh Ajlouni; Ammar F Mubaidin; Maha Till; Azmi Hadidi; Hatem El-Shanti; Kamel M Ajlouni
Journal:  Eur J Pediatr       Date:  2002-03       Impact factor: 3.183

Review 2.  International classification of osteochondrodysplasias. The International Working Group on Constitutional Diseases of Bone.

Authors:  J Spranger
Journal:  Eur J Pediatr       Date:  1992-06       Impact factor: 3.183

Review 3.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994

4.  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

  4 in total

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