Approach to a Child with Massive Hepatomegaly
Author:
Publisher
Jaypee Brothers Medical Publishing
Link
https://www.apgh.net/doi/pdf/10.5005/jp-journals-11009-0147
Reference6 articles.
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3. 3. Singh SK, Sarma MS. Hereditary fructose intolerance: a comprehensive review. World J Clin Pediatr 2022;11(4):321–329. DOI: 10.5409/wjcp.v11.i4.321
4. 4. Burton BK, Deegan PB, Enns GM, et al. Clinical features of lysosomal acid lipase deficiency. J Pediatr Gastroenterol Nutr 2015;61(6):619–625. DOI: 10.1097/MPG.0000000000000935
5. 5. Bay L, Canero Velasco C, Ciocca M, et al. Liver disease and dyslipidemia as a manifestation of lysosomal acid lipase deficiency (LAL-D). Clinical and diagnostic aspects, and a new treatment. An update. Arch Argent Pediatr 2017;115(3):287–293. DOI: 10.5546/aap.2017.eng.287
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