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[一名患有与帕陶氏综合征相关的唇裂患儿的麻醉]

[Anesthesia in a child operated for cleft lip associated with Patau's syndrome].

作者信息

Kamal Manoj, Varghese Don, Bhagde Jeet, Singariya Geeta, Simon Annie Miju, Singh Amar

机构信息

Dr. S.N. Medical College, Department of Anesthesia, Jodhpur, Rajasthan, Índia.

Jodhpur Dental College, Department of Oral and Maxillofacial Surgery, Jodhpur, Rajasthan, Índia.

出版信息

Braz J Anesthesiol. 2018 Mar-Apr;68(2):197-199. doi: 10.1016/j.bjan.2017.04.005. Epub 2017 May 16.

DOI:10.1016/j.bjan.2017.04.005
PMID:28526461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9391730/
Abstract

Patients with Patau's syndrome (Trisomy 13) have multiple craniofacial, cardiac, neurological and renal anomalies with very less life expectancy. Among craniofacial anomalies cleft lip and palate are common. These craniofacial and cardiac anomalies present difficulties with anesthesia. We therefore describe the anesthetic management in the case of a Trisomy 13 child for operated for cleft lip at 10 months of age.

摘要

患有帕陶氏综合征(13三体综合征)的患者存在多种颅面、心脏、神经和肾脏异常,预期寿命很短。在颅面异常中,唇腭裂很常见。这些颅面和心脏异常给麻醉带来了困难。因此,我们描述了一名10个月大接受唇裂手术的13三体综合征患儿的麻醉管理情况。

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本文引用的文献

1
Inpatient hospital care of children with trisomy 13 and trisomy 18 in the United States.美国 13 三体和 18 三体患儿的住院治疗。
Pediatrics. 2012 May;129(5):869-76. doi: 10.1542/peds.2011-2139. Epub 2012 Apr 9.
2
Better prognosis in newborns with trisomy 13 who received intensive treatments: a retrospective study of 16 patients.16 例接受强化治疗的 13 三体综合征新生儿的更好预后:一项回顾性研究。
Cell Biochem Biophys. 2012 Jul;63(3):191-8. doi: 10.1007/s12013-012-9355-0.
3
Clinical relevance of cytogenetics to pediatric practice. Postnatal findings of Patau syndrome - Review of 5 cases.细胞遗传学在儿科临床实践中的相关性。帕陶综合征的产后发现——5例病例回顾。
Maedica (Bucur). 2010 Jul;5(3):178-85.
4
Multiple congenital anomaly caused by an extra autosome.由额外常染色体引起的多重先天性异常。
Lancet. 1960 Apr 9;1(7128):790-3. doi: 10.1016/s0140-6736(60)90676-0.
5
Population-based analyses of mortality in trisomy 13 and trisomy 18.基于人群的13三体和18三体死亡率分析。
Pediatrics. 2003 Apr;111(4 Pt 1):777-84. doi: 10.1542/peds.111.4.777.
6
Long-term survival in Patau syndrome.帕陶综合征的长期存活情况。
Clin Dysmorphol. 2001 Apr;10(2):149-50. doi: 10.1097/00019605-200104000-00014.
7
Chromosomal abnormalities: trisomy 18, trisomy 13, deletions, and microdeletions.染色体异常:18三体、13三体、缺失及微缺失。
J Perinat Neonatal Nurs. 1999 Sep;13(2):59-75; quiz 103-4. doi: 10.1097/00005237-199909000-00006.
8
Anaesthesia for patients with trisomy 13 (Patau's syndrome).13三体综合征(帕陶氏综合征)患者的麻醉
Paediatr Anaesth. 1996;6(2):151-3. doi: 10.1111/j.1460-9592.1996.tb00380.x.
9
Natural history of trisomy 18 and trisomy 13: I. Growth, physical assessment, medical histories, survival, and recurrence risk.18三体和13三体的自然病史:I.生长发育、体格检查、病史、生存情况及复发风险。
Am J Med Genet. 1994 Jan 15;49(2):175-88. doi: 10.1002/ajmg.1320490204.
10
Rates of 47, + 13 amd 46 translocation D/13 Patau syndrome in live births and comparison with rates in fetal deaths and at amniocentesis.活产中47,+13及46易位型D/13帕陶综合征的发生率及其与死胎和羊膜穿刺术时发生率的比较。
Am J Hum Genet. 1980 Nov;32(6):849-58.