OzuahPOReznikM. Hepatomegaly In: McInernyTKAdamHMCampbellDEDeWittTGFoyJMKamatDM, eds. American Academy of Pediatrics Textbook of Pediatric Care. 2nd ed.Elk Grove Village, IL: American Academy of Pediatrics; 2017.
2.
PelizzoGGuazzottiMKlersyC, et al. Spleen size evaluation in children: time to define splenomegaly for pediatric surgeons and pediatricians. PLoS One. 2018;13:e0202741. doi:10.1371/journal.pone.0202741
SpencerNJ. Failure to think about failure to thrive. Arch Dis Child. 2006;92:95-96. doi:10.1136/adc.2006.098624
6.
Larson-NathCBiankVF. Clinical review of failure to thrive in pediatric patients. Pediatr Ann. 2016;45:e46-e49. doi:10.3928/00904481-20160114-01
7.
JaffeAC. Failure to thrive: current clinical concepts. Pediatr Rev. 2011;32:100-108. doi:10.1542/pir.32-3-100
8.
SaleemTHEltalawyHNAbu-FaddanNHAhmedAEGamalYHassanMH. Clinical and laboratory study on children with glycogen storage disease type-1 in upper Egypt. Adv Res Gastroenterol Hepatol. 2016;2:001-005. doi:10.19080/ARGH.2016.01.555578
9.
NgVL. Laboratory assessment of liver function and injury in children. In: SuchyFJSokolRJBalistreriWF, eds. Liver Disease in Children. 4th ed.Cambridge, England: Cambridge University Press; 2014:89.
10.
SchuchmanEHDesnickRJ. Types A and B Niemann-Pick disease. Mol Genet Metab. 2016;120:27-33. doi:10.1016/j.ymgme.2016.12.008
11.
SunA. Lysosomal storage disease overview. Ann Transl Med. 2018;6:476. doi:10.21037/atm.2018.11.39
12.
McGovernMMDionisi-ViciCGiuglianiRHwuPLidoveOLukacsZMengelKEMistryPKSchuchmanEHWassersteinMP. Consensus recommendation for a diagnostic guideline for acid sphingomyelinase deficiency. Genetics in Medicine. 2018;19:967-974.doi:10.1038/gim.2017.
