Suppr超能文献

莱施-奈恩病中的猝死。

Sudden death in Lesch-Nyhan disease.

作者信息

Neychev Vladimir Kostadinov, Jinnah H A

机构信息

Department of Neurology, Johns Hopkins Hospital, Baltimore, MD 21287, USA.

出版信息

Dev Med Child Neurol. 2006 Nov;48(11):923-6. doi: 10.1017/S0012162206002015.

Abstract

To increase awareness of sudden and unexpected death in Lesch-Nyhan disease (LND) and to explore its potential causes, we report the anteceding clinical features and laboratory evaluations of five males with LND who ultimately experienced sudden and unexpected death, along with three additional males who suffered serious respiratory events during life. The ages of patients ranged from 2 to 45 years. The cause of sudden death in LND appears to have a respiratory rather than a cardiogenic basis. All cases cannot be linked readily with a single respiratory process. Instead, different respiratory processes appear to operate in different cases. These may include aspiration, laryngospasm, central apnea, cyanotic breath-holding spells, and high cervical spine damage. Better recognition of these processes will help to guide appropriate workup and management that could include chest imaging, endoscopy of the airways, polysomnography, electroencephalogram, and brain and/or spine imaging.

摘要

为提高对莱施-奈恩病(LND)中猝死和意外死亡的认识,并探究其潜在病因,我们报告了五例最终猝死且死因意外的LND男性患者的前期临床特征和实验室评估结果,以及另外三例在生前发生严重呼吸事件的男性患者情况。患者年龄在2至45岁之间。LND猝死的原因似乎是呼吸系统而非心脏系统方面的。并非所有病例都能轻易与单一呼吸过程相关联。相反,不同病例中似乎存在不同的呼吸过程。这些过程可能包括误吸、喉痉挛、中枢性呼吸暂停、青紫型屏气发作以及高位颈椎损伤。更好地识别这些过程将有助于指导适当的检查和管理,其中可能包括胸部成像、气道内镜检查、多导睡眠图、脑电图以及脑部和/或脊柱成像。

相似文献

1
Sudden death in Lesch-Nyhan disease.
Dev Med Child Neurol. 2006 Nov;48(11):923-6. doi: 10.1017/S0012162206002015.
3
Multifocal atrophy of cerebellar internal granular neurons in lesch-nyhan disease: case reports and review.
J Neuropathol Exp Neurol. 2007 May;66(5):346-53. doi: 10.1097/nen.0b013e3180515319.
4
Brain white matter volume abnormalities in Lesch-Nyhan disease and its variants.
Neurology. 2015 Jan 13;84(2):190-6. doi: 10.1212/WNL.0000000000001128. Epub 2014 Dec 10.
6
Treatment of Lesch-Nyhan disease with S-adenosylmethionine: experience with five young Malaysians, including a girl.
Brain Dev. 2014 Aug;36(7):593-600. doi: 10.1016/j.braindev.2013.08.013. Epub 2013 Sep 18.
7
The motor disorder of classic Lesch-Nyhan disease.
Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1161-4. doi: 10.1081/NCN-200027432.
8
Behavioral aspects of Lesch-Nyhan disease and its variants.
Dev Med Child Neurol. 2005 Oct;47(10):673-7. doi: 10.1017/S0012162205001374.
9
Orthopedic problems in Lesch-Nyhan syndrome.
J Pediatr Orthop. 1999 Sep-Oct;19(5):596-602.
10
Protein metabolism in phenylketonuria and Lesch-Nyhan syndrome.
Pediatr Res. 1990 Sep;28(3):240-6. doi: 10.1203/00006450-199009000-00019.

引用本文的文献

1
Unleashing the Power of Induced Pluripotent stem Cells in in vitro Modelling of Lesch-Nyhan Disease.
Stem Cell Rev Rep. 2025 Feb;21(2):304-318. doi: 10.1007/s12015-024-10821-4. Epub 2024 Nov 4.
2
Delayed emergence from propofol anesthesia in a patient with Lesch-Nyhan syndrome: A case report.
Medicine (Baltimore). 2020 Aug 21;99(34):e21847. doi: 10.1097/MD.0000000000021847.
3
Phenotypic and molecular spectrum of Korean patients with Lesch-Nyhan syndrome and attenuated clinical variants.
Metab Brain Dis. 2019 Oct;34(5):1335-1340. doi: 10.1007/s11011-019-00441-0. Epub 2019 May 25.
4
Lesch-Nyhan syndrome: The saga of metabolic abnormalities and self-injurious behavior.
Intractable Rare Dis Res. 2017 Feb;6(1):65-68. doi: 10.5582/irdr.2016.01076.
6
Lesch-Nyhan Syndrome: Disorder of Self-mutilating Behavior.
Int J Clin Pediatr Dent. 2016 Apr-Jun;9(2):139-42. doi: 10.5005/jp-journals-10005-1350. Epub 2016 Jun 15.
7
The Effect of S-Adenosylmethionine on Self-Mutilation in a Patient with Lesch-Nyhan Disease.
JIMD Rep. 2017;32:51-57. doi: 10.1007/8904_2016_571. Epub 2016 Jun 14.
9
Fuzzy optimization for detecting enzyme targets of human uric acid metabolism.
Bioinformatics. 2013 Dec 15;29(24):3191-8. doi: 10.1093/bioinformatics/btt564. Epub 2013 Sep 26.
10
Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome.
Orphanet J Rare Dis. 2007 Dec 8;2:48. doi: 10.1186/1750-1172-2-48.

本文引用的文献

1
Laryngospasm in neurological diseases.
Neurocrit Care. 2006;4(2):163-7. doi: 10.1385/NCC:4:2:163.
2
Delineation of the motor disorder of Lesch-Nyhan disease.
Brain. 2006 May;129(Pt 5):1201-17. doi: 10.1093/brain/awl056. Epub 2006 Mar 20.
3
Laryngeal dystonia.
Otolaryngol Clin North Am. 2006 Feb;39(1):87-100. doi: 10.1016/j.otc.2005.11.001.
4
Behavioral aspects of Lesch-Nyhan disease and its variants.
Dev Med Child Neurol. 2005 Oct;47(10):673-7. doi: 10.1017/S0012162205001374.
6
The spectrum of mutations causing HPRT deficiency: an update.
Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1153-60. doi: 10.1081/NCN-200027400.
7
A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.
Am J Med. 1964 Apr;36:561-70. doi: 10.1016/0002-9343(64)90104-4.
9
Rapid eye movement sleep in breath holders.
J Child Neurol. 2000 Jul;15(7):449-52. doi: 10.1177/088307380001500705.
10
Lesch-Nyhan disease and the basal ganglia.
Brain Res Brain Res Rev. 2000 Apr;32(2-3):449-75. doi: 10.1016/s0165-0173(99)00094-6.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验