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Chromosomal Deletion in 7q31.2-31.32 Involving Ca2+-Dependent Activator Protein for Secretion Gene in a Patient with Cerebellar Ataxia: a Case Report.
Hong, Seungbeen; Lee, Su Ji; Cho, Sung-Rae.
Afiliação
  • Hong S; Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • Lee SJ; Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • Cho SR; Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, Korea.
Brain Neurorehabil ; 13(1): e9, 2020 Mar.
Article em En | MEDLINE | ID: mdl-36744273
ABSTRACT
We present a 33-year-old male patient with cerebellar ataxia. He was first considered to have a psychiatric conversion disorder but finally found to have chromosomal deletion in 7q31.2-31.32 involving Ca2+-dependent activator protein for secretion (CADPS) gene. When a targeted gene sequencing using next-generation sequencing panel and chromosomal microarray analysis were performed, an 8.6 Mb deletion within chromosome 7q31.2-31.32 was discovered. Deletion of CADPS gene in the 7q31.2-31.32 was suggested as the causative factor of cerebellar ataxia. Functional levels evaluated by Berg balance scale and modified Barthel index were improved via comprehensive rehabilitation including balance training and a dopamine agonist medication. To the best of our knowledge, this is the first report of chromosomal deletion in 7q31.2-31.32 including CADPS gene detected in patients with cerebellar ataxia.
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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Brain Neurorehabil Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Brain Neurorehabil Ano de publicação: 2020 Tipo de documento: Article