{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T03:22:37Z","timestamp":1761016957001,"version":"3.30.1"},"reference-count":16,"publisher":"Medknow","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Ann Med Health Sci Res"],"published-print":{"date-parts":[[2012]]},"DOI":"10.4103\/2141-9248.96946","type":"journal-article","created":{"date-parts":[[2012,6,5]],"date-time":"2012-06-05T16:23:46Z","timestamp":1338913426000},"page":"87","source":"Crossref","is-referenced-by-count":6,"title":["Clinical presentation of mucopolysaccharidosis type II (Hunter\u2032s syndrome)"],"prefix":"10.4103","volume":"2","author":[{"given":"JM","family":"Chinawa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"GN","family":"Adimora","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"HA","family":"Obu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B","family":"Tagbo","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F","family":"Ujunwa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I","family":"Onubogu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2581","reference":[{"key":"key-10.4103\/2141-9248.96946-1","first-page":"267","volume-title":"Mucopolysacharidosis type II: A clinical review and recommendation for treatment in the era of enzyme replacement therapy","author":"Wraith","year":"2008","journal-title":"Eur J Pediatr"},{"key":"key-10.4103\/2141-9248.96946-2","first-page":"377","volume-title":"Recognition and diagnosis of mucopolysacharidosis II","author":"Martin","year":"2008","journal-title":"Pediatrics"},{"key":"key-10.4103\/2141-9248.96946-3","first-page":"154","volume-title":"Atypical clinical presentation of mucopolysacharidosis type II: A case report","author":"Gauri","year":"2010","journal-title":"J Med Case Rep"},{"key":"key-10.4103\/2141-9248.96946-4","first-page":"169","volume-title":"Hunter syndrome: Case report and review of literature","author":"Ogunbiyi","year":"2006","journal-title":"West Afr J Med"},{"key":"key-10.4103\/2141-9248.96946-5","first-page":"270","volume-title":"Mucopolysacharidosis type II in females: A case report and review of literature","author":"Tuschi","year":"2005","journal-title":"Pediatr Neuro"},{"key":"key-10.4103\/2141-9248.96946-6","first-page":"104","volume-title":"A rare disease in two brothers","author":"Hunter","year":"1917","journal-title":"Proc R Soc Med"},{"key":"key-10.4103\/2141-9248.96946-7","unstructured":"Tarek B. Mucopolysaharidosis. Obtainable at e medicine specialties. [Last assessed on 2011 July 29 th ]."},{"key":"key-10.4103\/2141-9248.96946-8","unstructured":"Jurgen S. Mucopolysaccharidoses. In: Behrman RE, Kliegman EM, Jenson HB, editors. Nelson Textbook of Pediatrics. 18 th ed. Philadephia: Saunders; 2007. p. 620-6."},{"key":"key-10.4103\/2141-9248.96946-9","first-page":"234","volume-title":"Hunter syndrome: Presence of material cross reacting with antibodies against idorinate sulfatase","author":"Daniele","year":"1987","journal-title":"Hum Genet"},{"key":"key-10.4103\/2141-9248.96946-10","unstructured":"Alikor AD. Growth and development problem. In: Azubuike JC, Nkanginieme KE, editors. Paediatrics and child health in a tropical region. 2 nd ed. Owerri: African Educational Services; 2007. p. 76-7."},{"key":"key-10.4103\/2141-9248.96946-11","first-page":"179","volume-title":"Skin eruption as a presenting sign of hunter syndrome","author":"Demistsu","year":"1999","journal-title":"Clin Exp Dematol"},{"key":"key-10.4103\/2141-9248.96946-12","first-page":"377","volume-title":"Recognition and diagnosis of mucopolysacharidosis","author":"Rick","year":"2008","journal-title":"Am J Pediatr"},{"key":"key-10.4103\/2141-9248.96946-13","first-page":"518","volume-title":"Mitral vaive prolapse and type II mucopolysacharidosis.Report of two familial cases","author":"Sonino","year":"2001","journal-title":"Arch Mal Coeur Vaiss"},{"key":"key-10.4103\/2141-9248.96946-14","first-page":"481","volume-title":"The natural history of severe form of Hunter\u2032s disease: A study based on fifty two cases","author":"Young","year":"1983","journal-title":"Dev Med Child Neurol"},{"key":"key-10.4103\/2141-9248.96946-15","first-page":"837","volume-title":"Combined enzymatic and linkage analysis for heterozygote detection in hunters syndrome.Identification of an apparent case of germinal mosaicism","author":"Ben","year":"1993","journal-title":"Am J Med Gennet"},{"key":"key-10.4103\/2141-9248.96946-16","first-page":"365","volume-title":"Retinal pigmentary changes in mucopolysacharidoses of hunters type","author":"Danis","year":"1971","journal-title":"Bull Soc Belg Ophthalmol"}],"container-title":["Annals of Medical and Health Sciences Research"],"original-title":[],"language":"en","deposited":{"date-parts":[[2014,2,21]],"date-time":"2014-02-21T12:51:26Z","timestamp":1392987086000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.amhsr.org\/text.asp?2012\/2\/1\/87\/96946"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012]]},"references-count":16,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2012]]}},"alternative-id":["96946"],"URL":"https:\/\/doi.org\/10.4103\/2141-9248.96946","relation":{},"ISSN":["2141-9248"],"issn-type":[{"type":"print","value":"2141-9248"}],"subject":[],"published":{"date-parts":[[2012]]}}}