Literature DB >> 7695235

Early-onset ataxia with cardiomyopathy and retained tendon reflexes maps to the Friedreich's ataxia locus on chromosome 9q.

F Palau1, G De Michele, J J Vilchez, M Pandolfo, E Monrós, S Cocozza, P Smeyers, J Lopez-Arlandis, G Campanella, S Di Donato.   

Abstract

Absence of lower limb tendon reflexes has been considered an essential diagnostic criterion for Friedreich's ataxia (FA). However, preservation of knee and ankle jerks has been reported in a few patients. Linkage analysis to FA locus (FRDA) on chromosome 9q13-21.1 was performed in 11 patients from 6 families with FA phenotype, including cardiomyopathy, but retained reflexes (FARR). A maximal lod score of 3.38 at recombination fraction theta equal to 0.00 was obtained demonstrating that FARR maps to the FRDA locus. These results suggest that FARR is a variant phenotype of FA.

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Year:  1995        PMID: 7695235     DOI: 10.1002/ana.410370312

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  17 in total

Review 1.  Friedreich ataxia: an overview.

Authors:  M B Delatycki; R Williamson; S M Forrest
Journal:  J Med Genet       Date:  2000-01       Impact factor: 6.318

2.  Clinical heterogeneity of recessive ataxia in the Mexican population.

Authors:  A Rasmussen; M Gómez; E Alonso; S I Bidichandani
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-12       Impact factor: 10.154

Review 3.  The yeast connection to Friedreich ataxia.

Authors:  S A Knight; R Kim; D Pain; A Dancis
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 4.  The inherited ataxias and the new genetics.

Authors:  S R Hammans
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-10       Impact factor: 10.154

5.  Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.

Authors:  S I Bidichandani; T Ashizawa; P I Patel
Journal:  Am J Hum Genet       Date:  1997-05       Impact factor: 11.025

6.  Triplet repeat primed PCR (TP PCR) in molecular diagnostic testing for Friedreich ataxia.

Authors:  Paola Ciotti; Emilio Di Maria; Emilia Bellone; Franco Ajmar; Paola Mandich
Journal:  J Mol Diagn       Date:  2004-11       Impact factor: 5.568

7.  The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure.

Authors:  S I Bidichandani; T Ashizawa; P I Patel
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

8.  A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.

Authors:  P Smeyers; E Monrós; J Vílchez; J Lopez-Arlandis; F Prieto; F Palau
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

Review 9.  A pathogenetic classification of hereditary ataxias: is the time ripe?

Authors:  Giuseppe De Michele; Giovanni Coppola; Sergio Cocozza; Alessandro Filla
Journal:  J Neurol       Date:  2004-08       Impact factor: 4.849

10.  Frataxin gene point mutations in Italian Friedreich ataxia patients.

Authors:  Cinzia Gellera; Barbara Castellotti; Caterina Mariotti; Rossana Mineri; Viviana Seveso; Stefano Didonato; Franco Taroni
Journal:  Neurogenetics       Date:  2007-08-17       Impact factor: 2.660

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