Obstructive sleep apnea in familial partial lipodystrophy type 2 with atypical skin findings and vascular disease

Autor:	Debra Roseman, Heather N. Burbank, Hrayr Attarian, Kumar Patel
Rok vydání:	2009
Předmět:	medicine.medical_specialty Polysomnography medicine.medical_treatment DNA Mutational Analysis Coronary Artery Disease Disorders of Excessive Somnolence Internal medicine Body Fat Distribution Humans Medicine Carotid Stenosis Continuous positive airway pressure Sleep Apnea Obstructive Sleep disorder Continuous Positive Airway Pressure medicine.diagnostic_test business.industry Vascular disease Skin Diseases Genetic Sleep apnea Middle Aged Lamin Type A medicine.disease Familial partial lipodystrophy Lipodystrophy Familial Partial respiratory tract diseases Obstructive sleep apnea Phenotype Endocrinology Otorhinolaryngology Oxyhemoglobins Cardiology Female Neurology (clinical) Lipodystrophy Arousal business
Zdroj:	Sleep and Breathing. 13:425-427
ISSN:	1522-1709 1520-9512
DOI:	10.1007/s11325-009-0261-7
Popis:	A number of metabolic conditions have been associated with Obstructive Sleep Apnea Syndrome (OSAS). Familial partial lipodystrophy type 2 (FPLD2), one of the few rare genetic disorders affecting total body fat redistribution, is one of those conditions.In this case report the authors detail OSAS associated with FPLD2 with atypical dermatological and systemic manifestations.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e2edfb31ed32dd58cf64cd11a74f4d https://doi.org/10.1007/s11325-009-0261-7 Zobrazit plný text záznamu Full text from SpringerLink