Acute airway obstruction in Hunter syndrome

International Journal of Pediatric Otorhinolaryngology

Volumn 44, Issue 3, 1998, Pages 273-278

  Yoskovitch, Adi ^a   Tewfik, Ted L ^a,b   Brouillette, Robert T ^a   Schloss, Melvin D ^a   Der Kaloustian, Vazken M ^a  

^a MCGILL UNIVERSITY   (Canada)

^b MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

Hunter syndrome; Lysosomal enzyme; Tracheotomy

Indexed keywords

GLYCOSAMINOGLYCAN; IDURONATE 2 SULFATASE; LYSOSOME ENZYME;

AIRWAY OBSTRUCTION; ARTICLE; CASE REPORT; CHILD; ENZYME DEFICIENCY; FACIES; HUMAN; HUNTER SYNDROME; MACROGLOSSIA; MALE; MUCOPOLYSACCHARIDOSIS; NECK; PRIORITY JOURNAL; TRACHEOTOMY;

AIRWAY OBSTRUCTION; CHILD; HUMANS; MALE; MUCOPOLYSACCHARIDOSIS II; TRACHEOTOMY;

EID: 0032504711     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(98)00063-9     Document Type: Article

References (18)

1. [1] D. Baines, J. Keneally, Anaesthetic implications of the mucopolysaccharidoses: a fifteen year experience in a children's hospital, Anaesth. Intensive Care 11 (1983) 198-202.
2. [2] I. Brama, I. Gay, R. Feinmesser, et al., Upper airway obstruction in Hunter syndrome, Int. J. Pediatr. Otorhinolaryngol. 11 (1986) 229-235.
3. [3] T. Fujitani, A. Kimura, K. Inoue, et al., Pathological and biochemical study in the adenoid of mucopolysaccharidosis II, Int. J. Pediatr. Otorhinolaryngol. 10 (1985) 205-212.
4. [4] E. Hayes, R. Babin, C. Platz, The otologic manifestations of mucopolysaccharides, Am. J. Otol. 2 (1980) 65-69.
5. [5] R. Hopkins, J.A. Watson, J.H. Jones, et al., Two cases of Hunter's syndrome - The aneasthetic and operative difficulties in oral surgery, Br. J. Oral Surg. 10 (1973) 286-299.
6. [6] C. Hunter, A rare disease in two brothers, Proc. Roy. Soc. Med. 10 (1917) 104-116.
7. [7] D.H. King, R.M. Jones, M.B. Barnett, Anaesthetic considerations in the mucopolysaccharidoses, Anaesthesia 39 (1984) 126-131.
8. [8] A. Kreidstein, M.R. Boorin, J. Crespi, et al., Delayed awakening from anaesthesia in a patient with Hunter syndrome, Can. J. Anaesth. 41 (1994) 423-426.
9. [9] M. Kurihara, K. Kumagai, K. Goto, et al., Severe type Hunter's syndrome. Polysomnographic and neuropathological study, Neuropediatrics 23 (1992) 248-256.
10. [10] E. Le Guern, P. Couillin, I. Oberle, et al., More precise localization of the gene for Hunter syndrome, Genomics 7 (1990) 358-362.
11. [11] U.A. McKusick, R.R. Howell, L.E. Hussels, et al., Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses. Lancet I (1972) 993-996.
12. [12] J.M. Morehead, D.S. Parsons, Tracheobronchomalacia in Hunter's syndrome, Int. J. Pediatr. Otorhinolaryngol. 26 (1993) 255-261.
13. [13] C.T. Sasaki, R. Ruiz, R. Gaito Jr., et al., Hunter's syndrome: a study in airway obstruction, Laryngoscope 97 (1987) 280-285.
14. [14] G.L. Semenza, R.E. Pyeritz, Respiratory complications of mucopolysaccharide storage disorder, Medicine 67 (1988) 209-219.
15. [15] J. Shapiro, M. Strome, A.C. Crocker, Airway obstruction and sleep apnea in Hurler and Hunter syndromes, Ann. Otol. Rhinol. Laryngol. 94 (1985) 458-461.
16. [16] T.L. Tewfik, A.S. Teebi, V.M. Der Kaloustian, in: T.L. Tewfik, V.M. Der Kaloustian (Eds.), Selected Syndromes and Conditions In Congenital Anomalies of the Ear, Nose and Throat, Oxford University Press, New York, 1997, pp. 441-545.
17. [17] S. Yatziv, R.P. Erickson, C.J. Epstein, Mild and severe Hunter Syndrome (MPS II) within the same sibships, Clin. Genet. 11 (1977) 319-326.
18. [18] I.D. Young, P.S. Harper, Mild form of Hunter's syndrome: Clinical delineation based on 31 cases, Arch. Dis. Child. 57 (1982) 828-836.