Department of Sleep Medicine and Metabolic Disorders, Medical University of Lodz, 92-215 Lodz, Poland.
Int J Environ Res Public Health. 2021 Dec 20;18(24):13402. doi: 10.3390/ijerph182413402.
Congenital central hypoventilation syndrome (CCHS), also known as Ondine's curse, is a rare, potentially fatal genetic disease, manifesting as a lack of respiratory drive. Most diagnoses are made in pediatric patients, however late-onset cases have been rarely reported. Due to the milder symptoms at presentation that might easily go overlooked, these late-onset cases can result in serious health consequences later in life. Here, we present a case report of late-onset CCHS in an adolescent female patient. In this review we summarize the current knowledge about symptoms, as well as clinical management of CCHS, and describe in detail the molecular mechanism responsible for this disorder.
先天性中枢性低通气综合征(CCHS),又称奥丁诅咒,是一种罕见的、潜在致命的遗传性疾病,表现为呼吸驱动力缺失。大多数诊断都是在儿科患者中做出的,然而,迟发性病例很少有报道。由于发病时症状较轻,可能容易被忽视,这些迟发性病例可能会导致患者在以后的生活中出现严重的健康后果。在此,我们报告了一例青少年女性迟发性 CCHS 病例。在本次综述中,我们总结了目前关于 CCHS 的症状以及临床管理的知识,并详细描述了导致这种疾病的分子机制。