Anesthesia of a patient with Dubowitz syndrome -A case report-

Dubowitz syndrome is a rare autosomal recessive disorder that leads to growth retardation (intrauterine, postnatal), mental retardation, a peculiar face, microcephaly, behavioral problems and eczema. The peculiar face of individuals with Dubowitz syndrome includes sparse hair and eyebrows, low-set e...

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Main Authors: Min Kee Lee, Yong Seock Lee
Format: Article
Language:English
Published: Korean Society of Anesthesiologists 2010-05-01
Series:Korean Journal of Anesthesiology
Subjects:
Online Access:http://ekja.org/upload/pdf/kjae-58-495.pdf
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spelling doaj-e43e94218a2c4693be8e88081dc573d82020-11-25T03:58:21ZengKorean Society of AnesthesiologistsKorean Journal of Anesthesiology2005-64192005-75632010-05-0158549549910.4097/kjae.2010.58.5.4956908Anesthesia of a patient with Dubowitz syndrome -A case report-Min Kee Lee0Yong Seock Lee1Department of Anesthesiology and Pain Medicine, Korea Institute of Radiological & Medical Sciences, Seoul, Korea.Department of Anesthesiology and Pain Medicine, Korea Institute of Radiological & Medical Sciences, Seoul, Korea.Dubowitz syndrome is a rare autosomal recessive disorder that leads to growth retardation (intrauterine, postnatal), mental retardation, a peculiar face, microcephaly, behavioral problems and eczema. The peculiar face of individuals with Dubowitz syndrome includes sparse hair and eyebrows, low-set ears, blepharophimosis, bilateral ptosis, a flat nasal bridge with a broad nasal root and micrognathia. Airway management of such individuals might be difficult due to craniofacial anomalies, such as micrognathia, cleft palate, tooth problems and craniocervical anomalies. In addition, anesthetic management may be complicated by other systemic illnesses. We report the uneventful anesthetic management of a 16-year-old girl with Dubowitz syndrome who underwent a total abdominal hysterectomy after a pelvic examination under general anesthesia. We report this case of Dubowitz syndrome with a review of the relevant literature.http://ekja.org/upload/pdf/kjae-58-495.pdfairway managementcongenital anomalydubowitz syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Min Kee Lee
Yong Seock Lee
spellingShingle Min Kee Lee
Yong Seock Lee
Anesthesia of a patient with Dubowitz syndrome -A case report-
Korean Journal of Anesthesiology
airway management
congenital anomaly
dubowitz syndrome
author_facet Min Kee Lee
Yong Seock Lee
author_sort Min Kee Lee
title Anesthesia of a patient with Dubowitz syndrome -A case report-
title_short Anesthesia of a patient with Dubowitz syndrome -A case report-
title_full Anesthesia of a patient with Dubowitz syndrome -A case report-
title_fullStr Anesthesia of a patient with Dubowitz syndrome -A case report-
title_full_unstemmed Anesthesia of a patient with Dubowitz syndrome -A case report-
title_sort anesthesia of a patient with dubowitz syndrome -a case report-
publisher Korean Society of Anesthesiologists
series Korean Journal of Anesthesiology
issn 2005-6419
2005-7563
publishDate 2010-05-01
description Dubowitz syndrome is a rare autosomal recessive disorder that leads to growth retardation (intrauterine, postnatal), mental retardation, a peculiar face, microcephaly, behavioral problems and eczema. The peculiar face of individuals with Dubowitz syndrome includes sparse hair and eyebrows, low-set ears, blepharophimosis, bilateral ptosis, a flat nasal bridge with a broad nasal root and micrognathia. Airway management of such individuals might be difficult due to craniofacial anomalies, such as micrognathia, cleft palate, tooth problems and craniocervical anomalies. In addition, anesthetic management may be complicated by other systemic illnesses. We report the uneventful anesthetic management of a 16-year-old girl with Dubowitz syndrome who underwent a total abdominal hysterectomy after a pelvic examination under general anesthesia. We report this case of Dubowitz syndrome with a review of the relevant literature.
topic airway management
congenital anomaly
dubowitz syndrome
url http://ekja.org/upload/pdf/kjae-58-495.pdf
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