Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/55197
Title: Nonneurological Involvement in Late-Onset Friedreich Ataxia (LOFA): Exploring the Phenotypes
Authors: Martinez, Alberto R. M.
Moro, Adriana
Abrahao, Agessandro [UNIFESP]
Faber, Ingrid
Borges, Conrado R.
Rezende, Thiago J. R.
Martins, Carlos R., Jr.
Moscovich, Mariana
Munhoz, Renato P.
Segal, Sandra Leistner
Arruda, Walter O.
Saraiva-Pereira, Maria Luiza
Karuta, Simone
Pedroso, Jose Luiz [UNIFESP]
D'Abreu, Anelyssa
Jardim, Laura B.
Lopes-Cendes, Iscia
Barsottini, Orlando G. [UNIFESP]
Teive, Helio A. G.
Franca, Marcondes C., Jr.
Keywords: Late-onset Friedreich ataxia
Retained reflexes
Spastic ataxia
Ataxia
Issue Date: 2017
Publisher: Springer
Citation: Cerebellum. New York, v. 16, n. 1, p. 253-256, 2017.
Abstract: Friedreich's ataxia (FDRA) is the most common inherited ataxia worldwide, caused by homozygous GAA expansions in the FXN gene. Patients usually have early onset ataxia, areflexia, Babinski sign, scoliosis and pes cavus, but at least 25 % of cases have atypical phenotypes. Disease begins after the age of 25 in occasional patients (late-onset Friedreich ataxia (LOFA)). Little is known about the frequency and clinical profile of LOFA patients. One hundred six patients with molecular confirmation of FDRA and followed in three Brazilian outpatient centers were enrolled. General demographics, GAA expansion size, age at onset, cardiac, endocrine, and skeletal manifestations were evaluated and compared between LOFA and classic FDRA (cFDRA) groups. We used Mann-Whitney and Fisher tests to compare means and proportions between groups
p values < 0.05 were considered significant. LOFA accounted for 17 % (18/106) and cFDRA for 83 % (88/106) of the patients. There were 13 and 48 women in each group, respectively. LOFA patients were significantly older and had smaller GAA expansions. Clinically, LOFA group had a tendency toward lower frequency of diabetes/impaired glucose tolerance (5.8 vs. 17 %, p = 0.29) and cardiomyopathy (16.6 vs. 28.4 %, p = 0.38). Skeletal abnormalities were significantly less frequent in LOFA (scoliosis 22 vs. 61 %, p = 0.003, and pes cavus 22 vs.75 %, p < 0.001) as were spasticity and sustained reflexes, found in 22 % of LOFA patients but in none of the cFDRA patients (p = 0.001). LOFA accounts for 17 % of Brazilian FDRA patients evaluated herein. Clinically, orthopedic features and spasticity with retained reflexes are helpful tips to differentiate LOFA from cFDRA patients.
URI: https://repositorio.unifesp.br/handle/11600/55197
ISSN: 1473-4222
Other Identifiers: http://dx.doi.org/10.1007/s12311-015-0755-8
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