Visceral symptoms as a key diagnostic sign for the early infantile form of Niemann-Pick disease type C in a Russian patient: a case report

J Med Case Rep. 2016 Jun 1;10(1):143. doi: 10.1186/s13256-016-0925-4.

Abstract

Background: Niemann-Pick disease type C is a rare metabolic disease characterized by progressive neurological deterioration with childhood onset, and often results in premature mortality. Niemann-Pick disease type C has an extremely heterogeneous clinical presentation with a wide range of visceral and neurological signs and symptoms that are not specific to the disease, and which progress over varied periods of time. The incidence and epidemiology of Niemann-Pick disease type C in Russia have not been characterized. We report the case of a Russian newborn with early-infantile onset Niemann-Pick disease type C who displayed prolonged neonatal jaundice and hepatosplenomegaly.

Case presentation: A 5-year-old white boy born to non-consanguineous Russian parents was originally diagnosed with galactosemia at the age of 2 months based on a raised blood galactose level. A galactose-free and lactose-free diet resulted in achievement of a normal galactose level, but hepatosplenomegaly and cholestatic signs persisted. Liver biopsy results hinted at possible Niemann-Pick disease type C, but differential diagnostic investigations for progressive familial intrahepatic cholestasis type 2 (Byler syndrome) indicated a heterozygous genotype suggestive of this disease. Further, progressive neurological symptoms prompted additional genetic analyses for possible Niemann-Pick disease type C, from which an as-yet unreported combination of known NPC1 gene mutations was identified, and a final diagnosis of Niemann-Pick disease type C was established. The patient subsequently developed typical neurological symptoms of early-infantile Niemann-Pick disease type C, including vertical supranuclear ophthalmoparesis and cerebellar ataxia. Miglustat therapy was initiated 2.5 years ago, and some improvements in movement and speech have since been observed.

Conclusions: This case illustrates the continued challenges associated with diagnosing Niemann-Pick disease type C based on the appearance of nonspecific cholestatic symptoms. Based on this case we recommend examination of all newborns and children who display unexplained cholestasis or isolated splenomegaly/hepatosplenomegaly during the first months of life for other signs of possible Niemann-Pick disease type C.

Keywords: Cholestasis; Miglustat; Niemann–Pick disease type C; Splenomegaly.

Publication types

  • Case Reports

MeSH terms

  • 1-Deoxynojirimycin / analogs & derivatives
  • 1-Deoxynojirimycin / therapeutic use
  • Child, Preschool
  • Cholestasis, Intrahepatic / diagnosis*
  • Cholestasis, Intrahepatic / genetics
  • Cholestasis, Intrahepatic / pathology
  • Diagnostic Errors
  • Galactosemias / diagnosis*
  • Genetic Testing
  • Glycoside Hydrolase Inhibitors / therapeutic use
  • Hepatomegaly / etiology
  • Humans
  • Infant
  • Infant, Newborn
  • Jaundice, Neonatal / etiology
  • Liver / pathology*
  • Male
  • Niemann-Pick Disease, Type C / complications
  • Niemann-Pick Disease, Type C / diagnosis*
  • Niemann-Pick Disease, Type C / drug therapy
  • Niemann-Pick Disease, Type C / pathology
  • Russia
  • Splenomegaly / etiology

Substances

  • Glycoside Hydrolase Inhibitors
  • 1-Deoxynojirimycin
  • miglustat

Supplementary concepts

  • Cholestasis, progressive familial intrahepatic 1
  • Cholestasis, progressive familial intrahepatic 2