CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY
Supervisor：Ministry of Education of the People’s Republic of ChinaSponsor：West China Hospital, Sichuan University Editor-in-chief：Wu Hong Publishing period：
Monthly
ISSN：1007-9424CN：51-1505/R
Citation：巨家華, 董鶴翔, 俞永江. 黏多糖貯積癥Ⅰ型合并臍疝1例報道. CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY, 2023, 30(8): 978-979. doi: 10.7507/1007-9424.202303015Copy
Copyright ? the editorial department of CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY of West China Medical Publisher. All rights reserved
1.
Vasilev F, Sukhomyasova A, Otomo T. Mucopolysaccharidosis-plus syndrome. Int J Mol Sci, 2020, 21(2): 421. doi: 10.3390/ijms21020421.
2.
Tebani A, Zanoutene-Cheriet L, Adjtoutah Z, et al. Clinical and molecular characterization of patients with mucopolysaccharidosis typeⅠ in an Algerian Series. Int J Mol Sci, 2016, 17 (5): 743. doi: 10.3390/ijms17050743.
3.
Jameson E, Jones S, Remmington T. Enzyme replacement therapy with laronidase (Aldurazyme?) for treating mucopolysaccharidosis typeⅠ. Cochrane Database Syst Rev, 2019, 6(6): Cd009354. doi: 10.1002/14651858.CD009354.pub5.
4.
Giugliani R, Federhen A, Rojas MV, et al. MucopolysaccharidosisⅠ, Ⅱ, andⅥ: brief review and guidelines for treatment. Genet Mol Biol, 2010, 33(4): 589-604.
5.
Cantú-Reyna C, Vazquez-Cantu DL, Cruz-Camino H, et al. Mucopolysaccharidosis type Ⅰ in Mexico: case-based review. Children (Basel). 2023, 10(4): 642. doi: 10.3390/children10040642.
6.
Hulsebos RG, Zeebregts CJ, De Langen ZJ. Perforation of a congenital umbilical hernia in a patient with Hurler’s syndrome. J Pediatr Surg, 2004, 39(9): 1426-1427.
7.
Gurumurthy T, Shailaja S, Kishan S, et al. Management of an anticipated difficult airway in Hurler’s syndrome. J Anaesthesiol Clin Pharmacol, 2014, 30(4): 558-561.
8.
Mishra SR, Shastri M, Ramesh J. Role of rehabilitation in Hurler’s syndrome. J Back Musculoskelet Rehabil, 2017, 30(3): 635-639.
9.
Muenzer J, Wraith JE, Clarke LA, et al. MucopolysaccharidosisⅠ: management and treatment guidelines. Pediatrics, 2009, 123(1): 19-29.
1. Vasilev F, Sukhomyasova A, Otomo T. Mucopolysaccharidosis-plus syndrome. Int J Mol Sci, 2020, 21(2): 421. doi: 10.3390/ijms21020421.
2. Tebani A, Zanoutene-Cheriet L, Adjtoutah Z, et al. Clinical and molecular characterization of patients with mucopolysaccharidosis typeⅠ in an Algerian Series. Int J Mol Sci, 2016, 17 (5): 743. doi: 10.3390/ijms17050743.
3. Jameson E, Jones S, Remmington T. Enzyme replacement therapy with laronidase (Aldurazyme?) for treating mucopolysaccharidosis typeⅠ. Cochrane Database Syst Rev, 2019, 6(6): Cd009354. doi: 10.1002/14651858.CD009354.pub5.
4. Giugliani R, Federhen A, Rojas MV, et al. MucopolysaccharidosisⅠ, Ⅱ, andⅥ: brief review and guidelines for treatment. Genet Mol Biol, 2010, 33(4): 589-604.
5. Cantú-Reyna C, Vazquez-Cantu DL, Cruz-Camino H, et al. Mucopolysaccharidosis type Ⅰ in Mexico: case-based review. Children (Basel). 2023, 10(4): 642. doi: 10.3390/children10040642.
6. Hulsebos RG, Zeebregts CJ, De Langen ZJ. Perforation of a congenital umbilical hernia in a patient with Hurler’s syndrome. J Pediatr Surg, 2004, 39(9): 1426-1427.
7. Gurumurthy T, Shailaja S, Kishan S, et al. Management of an anticipated difficult airway in Hurler’s syndrome. J Anaesthesiol Clin Pharmacol, 2014, 30(4): 558-561.
8. Mishra SR, Shastri M, Ramesh J. Role of rehabilitation in Hurler’s syndrome. J Back Musculoskelet Rehabil, 2017, 30(3): 635-639.
9. Muenzer J, Wraith JE, Clarke LA, et al. MucopolysaccharidosisⅠ: management and treatment guidelines. Pediatrics, 2009, 123(1): 19-29.
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Citation：巨家華, 董鶴翔, 俞永江. 黏多糖貯積癥Ⅰ型合并臍疝1例報道. CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY, 2023, 30(8): 978-979. doi: 10.7507/1007-9424.202303015
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