Kennedy disease in Peru: First cases with molecular diagnosis
Original title: Kennedy disease in Peru: First cases with molecular diagnosis
- Víctor Gómez-Calero(corresponding author),
- ,
- Olimpio Ortega,
- Victoria Marca,
- Saúl Lindo-Samanamud,
- Martha Flores
- docencia y atención especializada en epilepsia,
- Northern Pacific Global Health Research Fellows Training Consortium
Research Output:
Contribution to journal
Article
Peer-reviewPublication Information
Output type
Research Output:
Contribution to journal
Article
Peer-reviewOriginal language
EnglishPages from-to (Number of pages)
Pages 331-335 (5 pages)Journal (Volume, Issue Number)
Revista Peruana de Medicina Experimental y Salud Publica (Volume 30, Issue 2)Publication milestones
- Published - 2013
Publication status
Published - 2013
ISSN
1726-4634Publication IDs
- Scopus: 84882720778
- PubMed: 23949524
Abstract
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 Kennedýs disease with confirmed molecular diagnosis.
Funding Details
FundersFunding numbers
FIC
R25TW009345
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Sustainable Development Goals
- SDG 3 Good Health and Well
