Perry syndrome with a novel mutation and a rare presentation: First report from India

Perry syndrome with a novel mutation and a rare presentation: First report from India

Objective: To characterize the first patient of Perry syndrome reported from India. Methods: A 62-year-old gentleman presented with acute encephalopathy, hypercapnia, central hypoventilation, and seizures. He required ventilatory support for persistent respiratory failure even after the resolution o...

Full description

Bibliographic Details
Main Authors: Pramod Krishnan, Gosala R K. Sarma, Uday Murgod, Murali Srinivas, Ajit K Roy
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Annals of Indian Academy of Neurology
Subjects:
autosomal dominant
central hypoventilation
dctn1 gene
parkinsonism
perry syndrome
weight loss
genetics
Online Access:http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=4;spage=703;epage=706;aulast=Krishnan

Internet

http://www.annalsofian.org/article.asp?issn=0972-2327;year=2022;volume=25;issue=4;spage=703;epage=706;aulast=Krishnan

Similar Items