Literature DB >> 22110888

The general anesthesia experience of deletion 8p syndrome patient -A case report-.

Woo Jong Shin1, Sang Duk Kim, Kyoung Hun Kim.   

Abstract

A deletion 8p syndrome is a relatively uncommon congenital disease characterized by mental retardation associated with multiple malformation that make anesthetic management a challenge. Anesthetic management of a patient with deletion 8p syndrome may pose a serious problem mainly from difficult tracheal intubation, aspiration complication and cardiac malformation. We experienced a case of 10 year-old boy with a deletion 8p syndrome who underwent appendectomy under the general anesthesia. Intubation was performed by video glidescope after unsuccessful attempt with Macintosh laryngoscope. A high arched palate, short neck, poor patient cooperation due to mental retardation and occasional autistic behaviour made airway management difficult. This case should alert anesthesiologists to the greater difficulties of managing patients with deletion 8p syndrome.

Entities:  

Keywords:  Congenital disease; Deletion 8p syndrome; Difficult intubation; Mental retardation

Year:  2011        PMID: 22110888      PMCID: PMC3219781          DOI: 10.4097/kjae.2011.61.4.332

Source DB:  PubMed          Journal:  Korean J Anesthesiol        ISSN: 2005-6419


  15 in total

Review 1.  Molecular cytogenetic analysis of a familial 8p23.1 deletion associated with minimal dysmorphic features, seizures, and mild mental retardation.

Authors:  M J Pettenati; N Rao; C Johnson; R Hayworth; K Crandall; O Huff; I T Thomas
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

2.  A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.

Authors:  I Claeys; M Holvoet; B Eyskens; P Adriaensens; M Gewillig; J P Fryns; K Devriendt
Journal:  Am J Med Genet       Date:  1997-09-19

Review 3.  Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature.

Authors:  L Faivre; N Morichon-Delvallez; G Viot; F Narcy; S Loison; L Mandelbrot; M C Aubry; V Raclin; P Edery; A Munnich; M Vekemans
Journal:  Prenat Diagn       Date:  1998-10       Impact factor: 3.050

4.  Deletion 8p syndrome.

Authors:  M C Digilio; B Marino; P Guccione; A Giannotti; R Mingarelli; B Dallapiccola
Journal:  Am J Med Genet       Date:  1998-02-17

5.  Anaesthetic implications of Cornelia de Lange syndrome.

Authors:  L M Corsini; G De Stefano; M C Porras; S Galindo; J Palencia
Journal:  Paediatr Anaesth       Date:  1998       Impact factor: 2.556

6.  Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndrome.

Authors:  K Devriendt; K De Mars; P De Cock; M Gewillig; J P Fryns
Journal:  Ann Genet       Date:  1995

7.  Difficult tracheal intubation in obstetrics.

Authors:  R S Cormack; J Lehane
Journal:  Anaesthesia       Date:  1984-11       Impact factor: 6.955

8.  Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13).

Authors:  B B de Vries; M Lees; S J Knight; R Regan; D Corney; J Flint; A Barnicoat; R M Winter
Journal:  Am J Med Genet       Date:  2001-04-01

9.  Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

Authors:  Margaret J Wat; Oleg A Shchelochkov; Ashley M Holder; Amy M Breman; Aditi Dagli; Carlos Bacino; Fernando Scaglia; Roberto T Zori; Sau Wai Cheung; Daryl A Scott; Sung-Hae Lee Kang
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

10.  8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.

Authors:  John C K Barber; Viv K Maloney; Shuwen Huang; David J Bunyan; Lara Cresswell; Esther Kinning; Anna Benson; Tim Cheetham; Jonathan Wyllie; Sally Ann Lynch; Simon Zwolinski; Laura Prescott; Yanick Crow; Rob Morgan; Emma Hobson
Journal:  Eur J Hum Genet       Date:  2007-10-17       Impact factor: 4.246

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  1 in total

Review 1.  Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.

Authors:  Zoe Papadopoulou; Ioannis Papoulidis; Stavros Sifakis; Georgios Markopoulos; Annalisa Vetro; Angeliki-Maria Vlaikou; Monica Ziegler; Thomas Liehr; Loretta Thomaidis; Orsetta Zuffardi; Maria Syrrou; Kitsos George; Emmanouil Manolakos
Journal:  Mol Med Rep       Date:  2017-10-10       Impact factor: 2.952

  1 in total

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