Autonomic failures in Perry syndrome with DCTN1 mutation

Sachiko Ohshima, Yoshio Tsuboi, Akifumi Yamamoto, Masato Kawakami, Matthew J. Farrer, Jun ichi Kira, Hirofumi Shii

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Perry syndrome is a familial parkinsonism associated with central hypoventilation, mental depression, and weight loss. Previously, this very rare syndrome has been reported in only 7 families worldwide including in one Japanese family. We recently identified an additional family with Perry syndrome with DCTN1 mutation residing in Japan. The pedigree contains 19 family members spanning three generations, with four affected individuals. Affected members with early stage disease in this family presented with marked autonomic dysfunction including orthostatic hypotension and decreased cardiac uptake with [123]I-metaiodobenzylguanidine scintigram features that have not been described in previous cases. Because of central hypoventilation, all affected members need ventilation assistance, which is thought beneficial for prolongation of survival time as well as improving quality of life in this syndrome.

Original languageEnglish
Pages (from-to)612-614
Number of pages3
JournalParkinsonism and Related Disorders
Volume16
Issue number9
DOIs
Publication statusPublished - Nov 2010

All Science Journal Classification (ASJC) codes

  • Neurology
  • Geriatrics and Gerontology
  • Clinical Neurology

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