Obstructive sleep apnea in patient with Prader-Willi syndrome

4Citations
Citations of this article
13Readers
Mendeley users who have this article in their library.

Abstract

Prader-Willi syndrome (PWS) is a genetic disorder caused by loss of function of genes situated within the 15q11-q13 region of chromosome 15. The disorder is characterized by central obesity, short stature, dysfunction of several hypothalamic centers. These symptoms lead to progressive metabolic, respiratory, circulatory and orthopedic complications. Because of the etiology of the disorder there is no known causal treatment. Patients should comply with dietary restrictions and behavioral modifications as it may reduce the risk of obesity related diseases. In this paper we present case of a 34-years old obese patient with PWS who was diagnosed with obstructive sleep apnea, and whom CPAP treatment was offered.

Cite

CITATION STYLE

APA

Czystowska, M., Skoczylas, A., Rudnicka, A., Kazanecka, B., Pływaczewski, R., Sliwiński, P., & Górecka, D. (2010). Obstructive sleep apnea in patient with Prader-Willi syndrome. Pneumonologia i Alergologia Polska : Organ Polskiego Towarzystwa Ftyzjopneumonologicznego, Polskiego Towarzystwa Alergologicznego, i Instytutu Gruźlicy i Chorób Płuc, 78(2), 148–152. https://doi.org/10.5603/arm.27738

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free