A Rare Cause of Cirrhosis in a Toddler

Author:

Raseena Jasna Nizar,Sobhan Prasanth KN,Sarasam Ajith K Ananda Krishnan

Publisher

Jaypee Brothers Medical Publishing

Reference8 articles.

1. 1. Massese M, Tagliaferri F, Dionisi-Vici C, et al. Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI. Orphanet J Rare Dis 2022;17(1):241. DOI: 10.1186/s13023-022-02387-6

2. 2. Sreekantam S, Rizvi H, Brown R, et al. An uncommon cause of early infantile liver disease and raised chitotriosidase. JIMD Rep 2020;54(1):22–24. DOI: 10.1002/jmd2.12123

3. 3. Chen Y. Glycogen storage disease. In: Scriver CR, Beaudet AS, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (Eds). The Metabolic and Molecular Basis of Inherited Disease, 8th edition. New York, NY: McGraw-Hill; 2001. pp. 1521–1551.

4. 4. Greene HL, Ghishan FK, Brown B, et al. Hypoglycemia in type IV glycogenosis: hepatic improvement in two patients with nutritional management. J Pediatr 1988;112(1):55–58. DOI: 10.1016/s0022-3476(88)80121-5

5. 5. Magoulas PL, EL-Hattab AW. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (Eds). Glycogen Storage Disease Type IV. 2013.

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