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Article

Autonomic failures in Perry syndrome with DCTN1 mutation.

Parkinsonism & related disorders - 1 Nov 2010

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

Abstract excerpt

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...

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Source

Identifiers

PMID: 20702129
DOI: 10.1016/j.parkreldis.2010.07.001

Genes

DCTN1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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