Transabdominal preperitoneal repair for an adolescent patient with Hunter syndrome: a case report
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Publisher
Springer Science and Business Media LLC
Link
http://link.springer.com/content/pdf/10.1186/s40792-019-0645-2.pdf
Reference18 articles.
1. Hunter C. A rare disease in two brothers. Proc R Soc Med. 1917;10:104–16.
2. Bach G, Eisenberg F Jr, Cantz M, Neufeld EF. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proc Natl Acad Sci USA. 1973;70:2134–8.
3. Lin HY, Chuang CK, Chen MR, Lin SJ, Chiu PC, Niu DM, et al. Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the Hunter Outcome Survey (HOS). Orphanet J Rare Dis. 2018;13:89.
4. Potts WJ, Riker WL, Lewis JE. The treatment of inguinal hernia infants and children. Ann Surg. 1950;132:566–74.
5. Takehara H, Yakabe S, Kameoka K. Laparoscopic percutaneous extraperitoneal closure for inguinal hernia in children: clinical outcome of 972 repairs done in 3 pediatric surgical institutions. J Pediatr Surg. 2006;41:1999–2003.
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