gastrointestinal symptoms in lysosmal disease

نویسندگان

farid imanzadeh 1.associate professor of pediatric gastroenterolgy, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, iran

چکیده

how to cite this article: imanzadeh f. gastrointestinal symptoms in lysosmal disease. iran j child neurol autumn 2012; 6:4 (suppl. 1):17-18. pls see pdf.   references: 1. semenza  gl,  pyeritz  re.  respiratory complications of mucopolysaccharide storage disorders. medicine (baltimore) 1988; 67:209. 2.   wraith   je,   scarpa   m,   beck   m,   et   al. mucopolysaccharidosis type ii (hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy. eur j pediatr 2008; 167:267. 3. stevens jm, kendall be, crockard ha, ransford   a.   the   odontoid   process   in morquio-brailsford’s disease. the effects of occipitocervical fusion. j bone joint surg br 1991; 73:851. 4.   jones ae, croley tf. morquio syndrome and anesthesia. anesthesiology 1979; 51:261. 5.   ashraf j, crockard ha, ransford ao, stevens jm. transoral decompression and posterior stabilisation in morquio’s disease. arch dis child 1991; 66:1318. 6.  neufeld ef, muenzer j. the metabolic and molecular bases of inherited disease, scriver c, beaudet al, valle d, sly w (eds), mcgraw- hill, new york 2001. p.3421. 7.   wraith   je.   the   mucopolysaccharidoses:   a clinical review and guide to management. arch dis child 1995; 72:263. 8.   cleary ma, wraith je. the presenting features of mucopolysaccharidosis type ih (hurler syndrome). acta paediatr 1995; 84:337. 9.   elsner b. ultrastructure of the rectal wall in hunter’s   syndrome.   gastroenterology   1970; 58:856. 10. cleary   ma,   wraith   je.   management   of mucopolysaccharidosis type iii. arch dis child 1993; 69:403.

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عنوان ژورنال:
iranian journal of child neurology

جلد ۶، شماره ۴، صفحات ۱۷-۱۸

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