Kennedy disease in Peru: first cases with molecular diagnosis
DOI:
https://doi.org/10.17843/rpmesp.2013.302.214Keywords:
Bulbo-spinal atrophy, X-linked, Receptors, androgen, Genetic diseasesAbstract
Kennedy’s disease is an X-linked recessive disorder with onset in adulthood, characterized by progressive degeneration of spinal motor neurons due to a dynamic mutation in the androgen receptor gene. We report three families (five cases) characterized by progressive weakness involving both limbs and bulbar muscles, atrophy, tremor, cramps and endocrinologic disturbances; the neurophysiological studies demonstrated second motor neuron impairment. The molecular analysis identified abnormal CAG repeats expansion in the androgen receptor gene (AR) in all cases. Clinical features were consistent with other previous reports. These are the first Peruvian cases of Kennedy ́s disease with confirmed molecular diagnosis.Downloads
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Published
2014-02-11
Issue
Section
Case Report
How to Cite
1.
Gómez-Calero V, Cornejo-Olivas M, Ortega O, Marca V, Lindo-Samanamud S, Flores M, et al. Kennedy disease in Peru: first cases with molecular diagnosis. Rev Peru Med Exp Salud Publica [Internet]. 2014 Feb. 11 [cited 2024 Dec. 24];30(2). Available from: https://rpmesp.ins.gob.pe/index.php/rpmesp/article/view/214