Literature DB >> 8684395

Ataxia without telangiectasia masquerading as benign hereditary chorea.

C Klein1, G K Wenning, N P Quinn, C D Marsden.   

Abstract

We report a nonconsanguineous family in whom two (of three) sons developed isolated chorea in early childhood, suggesting a diagnosis of benign hereditary chorea (BHC). However, cerebellar ataxia and oculomotor apraxia, without telangiectasia, subsequently developed. Chromosome analysis showed increased radiosensitivity in both brothers and translocations in the younger one. We conclude that ataxia with chromosomal instability may masquerade as BHC in some patients.

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Year:  1996        PMID: 8684395     DOI: 10.1002/mds.870110217

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  10 in total

Review 1.  Molecular pathology of ataxia telangiectasia.

Authors:  A M R Taylor; P J Byrd
Journal:  J Clin Pathol       Date:  2005-10       Impact factor: 3.411

Review 2.  New autosomal recessive cerebellar ataxias with oculomotor apraxia.

Authors:  Isabelle Le Ber; Alexis Brice; Alexandra Dürr
Journal:  Curr Neurol Neurosci Rep       Date:  2005-09       Impact factor: 5.081

Review 3.  Ataxia-telangiectasia - A historical review and a proposal for a new designation: ATM syndrome.

Authors:  Hélio A G Teive; Adriana Moro; Mariana Moscovich; Walter O Arruda; Renato P Munhoz; Salmo Raskin; Tetsuo Ashizawa
Journal:  J Neurol Sci       Date:  2015-05-29       Impact factor: 3.181

Review 4.  DNA repair abnormalities leading to ataxia: shared neurological phenotypes and risk factors.

Authors:  Edward C Gilmore
Journal:  Neurogenetics       Date:  2014-07-20       Impact factor: 2.660

Review 5.  Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?

Authors:  P J Brooks; Tsu-Fan Cheng; Lori Cooper
Journal:  DNA Repair (Amst)       Date:  2008-03-12

6.  Prominent oromandibular dystonia and pharyngeal telangiectasia in atypical ataxia telangiectasia.

Authors:  Fatima Carrillo; Susanne A Schneider; A Malcolm R Taylor; Venkataramanan Srinivasan; Raj Kapoor; Kailash P Bhatia
Journal:  Cerebellum       Date:  2009-03       Impact factor: 3.847

Review 7.  Recent advances in genetics of chorea.

Authors:  Niccolò E Mencacci; Miryam Carecchio
Journal:  Curr Opin Neurol       Date:  2016-08       Impact factor: 5.710

Review 8.  Nijmegen breakage syndrome (NBS).

Authors:  Krystyna H Chrzanowska; Hanna Gregorek; Bożenna Dembowska-Bagińska; Maria A Kalina; Martin Digweed
Journal:  Orphanet J Rare Dis       Date:  2012-02-28       Impact factor: 4.123

Review 9.  Autosomal recessive cerebellar ataxias.

Authors:  Francesc Palau; Carmen Espinós
Journal:  Orphanet J Rare Dis       Date:  2006-11-17       Impact factor: 4.123

10.  Ataxia-telangiectasia-like disorder in a family deficient for MRE11A, caused by a MRE11 variant.

Authors:  Maryam Sedghi; Mehri Salari; Ali-Reza Moslemi; Ariana Kariminejad; Mark Davis; Hayley Goullée; Björn Olsson; Nigel Laing; Homa Tajsharghi
Journal:  Neurol Genet       Date:  2018-12-03
  10 in total

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