Literature DB >> 12833395

Athabascan brainstem dysgenesis syndrome.

Steve Holve1, Barbara Friedman, H Eugene Hoyme, Theodore J Tarby, Sharon J Johnstone, Robert P Erickson, Carol L Clericuzio, Christopher Cunniff.   

Abstract

We report a new disorder with diverse neurological problems resulting from abnormal brainstem function. Consistent features of this disorder, which we propose should be called the Atabascan brainstem dysgenesis syndrome, include horizontal gaze palsy, sensorineural deafness, central hypoventilation, and developmental delay. Other features seen in some patients include swallowing dysfunction, vocal cord paralysis, facial paresis, seizures, and cardiac outflow tract anomalies. All affected children described are of Athabascan Indian heritage, with eight children from the Navajo tribe and two patients who are of Apache background. The disorder can be distinguished from the Moebius syndrome by the pattern of central nervous system findings, especially the sensorineural deafness, horizontal gaze palsy, and central hypoventilation. Recognition of children with some features of Athabascan brainstem dysgenesis syndrome should prompt investigation for other related abnormalities. Published 2003 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2003        PMID: 12833395     DOI: 10.1002/ajmg.a.20087

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


  18 in total

1.  Analysis of the CHN1 gene in patients with various types of congenital ocular motility disorders.

Authors:  Alexander E Volk; Julia Fricke; Judith Strobl; Gerold Kolling; Christian Kubisch; Antje Neugebauer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2010-06-10       Impact factor: 3.117

Review 2.  The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease.

Authors:  Carolyn P Graeber; David G Hunter; Elizabeth C Engle
Journal:  Semin Ophthalmol       Date:  2013 Sep-Nov       Impact factor: 1.975

3.  The clinical spectrum of homozygous HOXA1 mutations.

Authors:  Thomas M Bosley; Ibrahim A Alorainy; Mustafa A Salih; Hesham M Aldhalaan; Khaled K Abu-Amero; Darren T Oystreck; Max A Tischfield; Elizabeth C Engle; Robert P Erickson
Journal:  Am J Med Genet A       Date:  2008-05-15       Impact factor: 2.802

Review 4.  Recent progress in understanding congenital cranial dysinnervation disorders.

Authors:  Darren T Oystreck; Elizabeth C Engle; Thomas M Bosley
Journal:  J Neuroophthalmol       Date:  2011-03       Impact factor: 3.042

5.  Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.

Authors:  Janet C Rucker; Bryn D Webb; Tamiesha Frempong; Harald Gaspar; Thomas P Naidich; Ethylin Wang Jabs
Journal:  Brain       Date:  2014-02-21       Impact factor: 13.501

6.  Cardiovascular defects in a mouse model of HOXA1 syndrome.

Authors:  Nadja Makki; Mario R Capecchi
Journal:  Hum Mol Genet       Date:  2011-09-22       Impact factor: 6.150

7.  Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect.

Authors:  Amélie Pinard; Nathalie Eudes; Julia Mitchell; Fanny Bajolle; Maude Grelet; Joséphine Okoronkwo; Damien Bonnet; Gwenaelle Collod-Béroud; Stéphane Zaffran
Journal:  Mol Biol Rep       Date:  2018-06-19       Impact factor: 2.316

8.  HOXA1 mutations are not a common cause of Möbius syndrome.

Authors:  Jessica K Rankin; Caroline Andrews; Wai-Man Chan; Elizabeth C Engle
Journal:  J AAPOS       Date:  2010-02       Impact factor: 1.220

9.  Clinical characterization of the HOXA1 syndrome BSAS variant.

Authors:  T M Bosley; M A Salih; I A Alorainy; D T Oystreck; M Nester; K K Abu-Amero; M A Tischfield; E C Engle
Journal:  Neurology       Date:  2007-09-18       Impact factor: 9.910

Review 10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.