Airway-Related Symptoms and Surgeries in Patients With Mucopolysaccharidosis I

被引:39
作者
Am, Pamela [1 ]
Bruce, Iain A. [2 ,3 ]
Wraith, James E. [4 ]
Travers, Helen [5 ]
Fallet, Shari [5 ]
机构
[1] Nemours Childrens Clin, Dept Genet, Jacksonville, FL 32207 USA
[2] Royal Manchester Childrens Hosp, Cent Manchester Univ Hosp NHS Fdn Trust, Paediat ENT Dept, Manchester M27 1HA, Lancs, England
[3] Univ Manchester, Resp & Allergy Ctr, Inst Inflammat & Repair, Manchester, Lancs, England
[4] St Marys Hosp, Cent Manchester Univ Hosp NHS Fdn Trust, Manchester Ctr Genom Med, Willink Biochem Genet Unit, Manchester M13 0JH, Lancs, England
[5] Genzyme Sanofi Co, Cambridge, MA USA
关键词
airway; mucopolysaccharidosis I; registries; surgeries; symptoms; REGISTRY; MPS; MANAGEMENT; DIAGNOSIS;
D O I
10.1177/0003489414550154
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Mucopolysaccharidosis I (MPS I) is a progressive, debilitating, and life-threatening genetic disease, which, owing to the nonspecific nature of the early symptoms, is often unrecognized and associated with significant diagnostic delays. To improve early recognition leading to early diagnosis and initiation of treatment, we characterized the extent of airway-related symptoms and surgeries among patients with MPS I. Methods: Analysis of the frequency of airway-related symptoms and surgeries from 1041 patients enrolled in the MPS I Registry and correlation with other systemic manifestations of MPS I. Results: Airway-related symptoms (macroglossia, enlarged tonsils, reactive airway disease/asthma, or sleep disturbances) were reported for as many as 85% of Hurler, 83% of Hurler-Scheie, and 65% of Scheie patients very often before the diagnosis of MPS I was established. Surgeries for an airway indication were reported in 39% of patients and many had at least I airway-related surgery before the diagnosis of MPS I was confirmed. The mean percentage of patients with airway-related symptoms for whom hernias and/or dysostosis multiplex were also reported was 84% and 54%, respectively. Conclusion: Airway-related symptoms and surgeries are common and often the earliest presenting feature in MPS I. Improved recognition of early MPS I disease manifestations may lead to earlier diagnosis and treatment.
引用
收藏
页码:198 / 205
页数:8
相关论文
共 15 条
[1]   High rate of postoperative mortality in patients with mucopolysaccharidosis I: findings from the MPS I Registry [J].
Arn, Pamela ;
Whitley, Chester ;
Wraith, J. Edmond ;
Webb, H. Warner ;
Underhill, Lisa ;
Rangachari, Lakshmi ;
Cox, Gerald F. .
JOURNAL OF PEDIATRIC SURGERY, 2012, 47 (03) :477-484
[2]   Characterization of Surgical Procedures in Patients with Mucopolysaccharidosis Type I: Findings from the MPS I Registry [J].
Arn, Pamela ;
Wraith, J. Edmond ;
Underhill, Lisa .
JOURNAL OF PEDIATRICS, 2009, 154 (06) :859-864
[3]   The natural history of MPS I: global perspectives from the MPS I Registry [J].
Beck, Michael ;
Arn, Pamela ;
Giugliani, Roberto ;
Muenzer, Joseph ;
Okuyama, Torayuki ;
Taylor, John ;
Fallet, Shari .
GENETICS IN MEDICINE, 2014, 16 (10) :759-765
[4]  
Chan Ying-Lun, 2001, Acta Paediatrica Taiwanica, V42, P306
[5]  
Cormier R.E., 1990, Clinical methods: The history, physical, and laboratory examinations, V3rd, P398
[6]   Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry [J].
D'Aco, Kristin ;
Underhill, Lisa ;
Rangachari, Lakshmi ;
Arn, Pamela ;
Cox, Gerald F. ;
Giugliani, Roberto ;
Okuyama, Torayuki ;
Wijburg, Frits ;
Kaplan, Paige .
EUROPEAN JOURNAL OF PEDIATRICS, 2012, 171 (06) :911-919
[7]   Enzyme replacement therapy and/or hematopoietic stem cell transplantation at diagnosis in patients with mucopolysaccharidosis type I: results of a European consensus procedure [J].
de Ru, Minke H. ;
Boelens, Jaap J. ;
Das, Anibh M. ;
Jones, Simon A. ;
van der Lee, Johanna H. ;
Mahlaoui, Nizar ;
Mengel, Eugen ;
Offringa, Martin ;
O'Meara, Anne ;
Parini, Rossella ;
Rovelli, Attilio ;
Sykora, Karl-Walter ;
Valayannopoulos, Vassili ;
Vellodi, Ashok ;
Wynn, Robert F. ;
Wijburg, Frits A. .
ORPHANET JOURNAL OF RARE DISEASES, 2011, 6
[8]   An algorithm to predict phenotypic severity in mucopolysaccharidosis type I in the first month of life [J].
Kingma, Sandra D. K. ;
Langereis, Eveline J. ;
de Klerk, Clasine M. ;
Zoetekouw, Lida ;
Wagemans, Tom ;
Ijlst, Lodewijk ;
Wanders, Ronald J. A. ;
Wijburg, Frits A. ;
van Vlies, Naomi .
ORPHANET JOURNAL OF RARE DISEASES, 2013, 8
[9]   Incidence of the Mucopolysaccharidoses in Taiwan, 1984-2004 [J].
Lin, Hsiang-Yu ;
Lin, Shuan-Pei ;
Chuang, Chih-Kuang ;
Niu, Dau-Ming ;
Chen, Ming-Ren ;
Tsai, Fuu-Jen ;
Chao, Mei-Chyn ;
Chiu, Pao-Ching ;
Lin, Shio-Jean ;
Tsai, Li-Ping ;
Hwu, Wuh-Liang ;
Lin, Ju-Li .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2009, 149A (05) :960-964
[10]   Mucopolysaccharidosis I: Management and Treatment Guidelines [J].
Muenzer, Joseph ;
Wraith, James E. ;
Clarke, Lorne A. .
PEDIATRICS, 2009, 123 (01) :19-29