Niemann-Pick Disease Type C Misdiagnosed as Cerebral Palsy: A Case Report
1
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Niemann-Pick disease type C (NP-C) is a rare autosomal recessive neurovisceral lysosomal lipid storage disorder. The clinical manifestations of the disorder are variable. This report describes the case of a 27-month-old girl with NP-C whose condition had been misdiagnosed as spastic cerebral palsy (CP). She had spasticity, particularly at both ankles, and gait disturbance. Magnetic resonance imaging of the brain revealed findings suspicious of sequelae from a previous insult, such as periventricular leukomalacia, leading to the diagnosis of CP. However, she had a history of hepatosplenomegaly when she was a fetus and her motor development had deteriorated, with symptoms of vertical supranuclear gaze palsy, cataplexy, and ataxia developing gradually. Therefore, NP-C was considered and confirmed with a genetic study, which showed mutation of the NPC1 gene. Thus, if a child with CP-like symptoms presents with a deteriorating course and NP-C-specific symptoms, NP-C should be cautiously considered.
Abstract
Niemann-Pick disease type C (NP-C) is a rare autosomal recessive neurovisceral lysosomal lipid storage disorder. The clinical manifestations of the disorder are variable. This report describes the case of a 27-month-old girl with NP-C whose condition had been misdiagnosed as spastic cerebral palsy (CP). She had spasticity, particularly at both ankles, and gait disturbance. Magnetic resonance imaging of the brain revealed findings suspicious of sequelae from a previous insult, such as periventricular leukomalacia, leading to the diagnosis of CP. However, she had a history of hepatosplenomegaly when she was a fetus and her motor development had deteriorated, with symptoms of vertical supranuclear gaze palsy, cataplexy, and ataxia developing gradually. Therefore, NP-C was considered and confirmed with a genetic study, which showed mutation of the NPC1 gene. Thus, if a child with CP-like symptoms presents with a deteriorating course and NP-C-specific symptoms, NP-C should be cautiously considered.
참고문헌 (10)
- Patterson MC, "Recommendations for the diagnosis and management of Niemann-Pick disease type C : an update", Mol Genet Metab, 106, pp.330~344 (2012)
- Lloyd-Evans E, "Lipids on trial : the search for the offending metabolite in Niemann-Pick type C disease", Traffic, 11, pp.419~428 (2010)
- Vanier MT, "Niemann-Pick disease type C", Orphanet J Rare Dis, 5, pp.16~ (2010)
- Rosenbaum P, "A report : the definition and classification of cerebral palsy April 2006", Dev Med Child Neurol Suppl, 109, pp.8~14 (2007)
- Wijburg FA, "Development of a suspicion index to aid diagnosis of Niemann-Pick disease type C", Neurology, 78, pp.1560~1567 (2012)
- Salsano E, "Vertical supranuclear gaze palsy in Niemann-Pick type C disease", Neurol Sci, 33, pp.1225~1232 (2012)
- Nevsimalova S, "Cataplexy and sleep disorders in Niemann-Pick type C disease", Curr Neurol Neurosci Rep, 15, pp.522~ (2015)
- Huang JY, "Neuroimaging findings in a brain with Niemann-Pick type C disease", J Formos Med Assoc, 110, pp.537~542 (2011)
- Walterfang M, "Subcortical volumetric reductions in adult Niemann-Pick disease type C : a cross-sectional study", AJNR Am J Neuroradiol, 34, pp.1334~1340 (2013)
- Walterfang M, "Pontine-to-midbrain ratio indexes ocular-motor function and illness stage in adult Niemann-Pick disease type C", Eur J Neurol, 19, pp.462~467 (2012)
