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Volume 6 Journal of Child and Adolescent Behavior
October 01-02, 2018 Osaka, Japan
3rd World Congress on
Pediatric Neurology and Pediatric Surgery
Neuropediatrics 2018
October 01-02, 2018
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in
SCARB2 gene and literature review
Wo-Tu Tian, Xiao-Li Liu, Xing-Hua Luan and Li Cao
Shanghai Jiao Tong University, China
Statement of the Problem: To describe the clinical and genetic features of a Chinese progressive myoclonus epilepsy (PME)
patient with SCARB2 mutation without renal impairment and review 27 SCARB2-related PME patients from 11 countries.
Method: The patient was a 27-year-old man with progressive action myoclonus, ataxia, epilepsy, dysarthria and absence of
cognitive deterioration. Renal functional test was normal. Electroencephalography showed progressively slowed background
activity and sporadic generalized spike-and-wave discharges. Electromyography showed slowed motor and sensory nerve
conduction velocities and distal motor latency delay accompanied by normal Compound Motor Action Potential (CMAP) and
amplitudes of Sensory Nerve Action Potential (SNAP). The amplitude of cortical components of Brainstem Auditory-Evoked
Potential (BAEP) was normal with slightly prolonged latencies. Generalized atrophy, ventricle enlargement and white matter
degeneration was observed in brain magnetic resonance imaging. Open muscle biopsy and genetic analysis were performed.
200 healthy individuals were set for control. qPCR, western blotting and immunofluorescence were carried out to evaluate the
fate of the SCARB2 mRNA and lysosomal-membrane type 2 (LIMP2) protein level.
Findings: One homozygous mutation in SCARB2 gene (c.1187+5G>T) was identified in the patient. Each of his parents carried
a heterozygous variant. This mutation was not detected in healthy controls and predicted to be disease causing by prediction
tools. qPCR revealed a significantly lower level of SCARB2 mRNA in peripheral blood cell of the proband compared with his
parents and healthy control. Muscle biopsy showed mild variation in fiber size. Western blotting and immunofluorescence
detected an extremely weak signal of LIMP2 protein from skeletal muscle of the proband.
Conclusion: In this study, we identified a SCARB2-related PME patient with normal renal function and a novel homozygous
splicing mutation. SCARB2 gene should be analyzed in patients with progressive action myoclonus, epilepsy, peripheral
neuropathy, without cognitive deterioration or renal failure.
J Child Adolesc Behav 2018, Volume 6
DOI: 10.4172/2375-4494-C1-006