Anesthetic implications of Jacobsen syndrome

被引:7
作者
Easley, RB
Sanders, D
McElrath-Schwartz, J
Martin, J
Redmond, JM
机构
[1] Johns Hopkins Med Inst, Dept Anesthesiol & Crit Care, Div Pediat Anesthesiol & Crit Care, Baltimore, MD 21287 USA
[2] Johns Hopkins Med Inst, Dept Surg, Div Cardiothorac Surg, Baltimore, MD 21287 USA
[3] Our Ladys Hosp Sick Children, Dublin 12, Ireland
关键词
anesthesia; Jacobsen syndrome; 11q-syndrome; Paris-Trousseau thrombocytopenia syndrome; 11q terminal deletion disorder; cardiac surgery;
D O I
10.1111/j.1460-9592.2005.01597.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Jacobsen syndrome (JS), also known as 11q-syndrome, is a congenital disorder associated with a deletion of the long arm of chromosome 11. Patients with JS characteristically exhibit multiple dysmorphic features, developmental delay, cardiac anomalies, and platelet abnormalities. Anesthetic issues related to the care of patients with JS concern airway management secondary to short neck, abnormal mouth shape and micrognathia/retrognathia, a high incidence of cardiac anomalies, and platelet dysfunction. Importantly, platelet abnormalities affect 95% of reported JS patients and involve platelet number, size and function. Two children with JS who required open heart surgery are presented and anesthetic management issues discussed. These patients represent the first reports regarding the perioperative issues in caring for patients with JS.
引用
收藏
页码:66 / 71
页数:6
相关论文
共 16 条
[1]   Specific genetic diseases at risk for sedation/anesthesia complications [J].
Butler, MG ;
Hayes, BG ;
Hathaway, MM ;
Begleiter, ML .
ANESTHESIA AND ANALGESIA, 2000, 91 (04) :837-855
[2]   Efficacy of aprotinin, epsilon aminocaproic acid, or combination in cyanotic heart disease [J].
Chauhan, S ;
Kumar, BA ;
Rao, BH ;
Rao, MS ;
Dubey, B ;
Saxena, N ;
Venugopal, P .
ANNALS OF THORACIC SURGERY, 2000, 70 (04) :1308-1312
[3]   The 11q terminal deletion disorder: A prospective study of 110 cases [J].
Grossfeld, PD ;
Mattina, T ;
Lai, Z ;
Favier, R ;
Jones, KL ;
Cotter, F ;
Jones, C .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 129A (01) :51-61
[4]   Endocrine abnormalities in patients with Jacobsen (11q-) syndrome [J].
Haghi, M ;
Dewan, A ;
Jones, KL ;
Reitz, R ;
Jones, C ;
Grossfeld, P .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 129A (01) :62-63
[5]   (11-21) TRANSLOCATION IN 4 GENERATIONS WITH CHROMOSOME 11 ABNORMALITIES IN OFFSPRING - CLINICAL, CYTOGENETICAL, AND GENE MARKER STUDY [J].
JACOBSEN, P ;
HAUGE, M ;
HENNINGSEN, K ;
HOBOLTH, N ;
MIKKELSEN, M ;
PHILIP, J .
HUMAN HEREDITY, 1973, 23 (06) :568-585
[6]   Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome:: evidence for a common mechanism of chromosome breakage [J].
Jones, C ;
Müllenbach, R ;
Grossfeld, P ;
Auer, R ;
Favier, R ;
Chien, K ;
James, M ;
Tunnacliffe, A ;
Cotter, F .
HUMAN MOLECULAR GENETICS, 2000, 9 (08) :1201-1208
[7]   2 CRANIOSYNOSTOTIC PATIENTS WITH 11Q DELETIONS, AND REVIEW OF 48 CASES [J].
LEWANDA, AF ;
MORSEY, S ;
REID, CS ;
JABS, EW .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 59 (02) :193-198
[8]   The anesthetic management of a patient with Cohen syndrome [J].
Meng, L ;
Quinlan, JJ ;
Sullivan, E .
ANESTHESIA AND ANALGESIA, 2004, 99 (03) :697-698
[9]  
Nargozian C, 2004, PEDIATR ANESTH, V14, P53, DOI 10.1046/j.1460-9592.2003.01200.x
[10]  
PENNY LA, 1995, AM J HUM GENET, V56, P676