黏多糖贮积症Ⅰ型合并脐疝1例报道_CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY

Authors：

巨家华 ¹ , 董鹤翔 ¹ ,  俞永江 ^1,2

1. ;
2. ;

Corresponding author：

俞永江, Email: ylongy@163.com

Keywords：

黏多糖贮积症; 脐疝; 疝修补术

DOI：

10.7507/1007-9424.202303015

Video：

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Citation： 巨家华, 董鹤翔, 俞永江. 黏多糖贮积症Ⅰ型合并脐疝1例报道. CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY, 2023, 30(8): 978-979. doi: 10.7507/1007-9424.202303015 Copy

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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黏多糖贮积症Ⅰ型合并脐疝1例报道

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