Displaying publications 1 - 20 of 54 in total

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  1. Khoo CS
    Am J Case Rep, 2018 Jul 24;19:864-867.
    PMID: 30038209 DOI: 10.12659/AJCR.909884
    BACKGROUND Dengue-associated neurological manifestations have recently been on the rise. Cerebellar syndrome complicating dengue fever has rarely been reported in the literature. We present a case report of dengue-associated cerebellar syndrome and performed a literature review to draw attention to this rare neurological complication. CASE REPORT A 60-year-old man presented with 4 days of fever, myalgia, arthralgia, headaches, and warning symptoms (persistent diarrhea and vomiting). He was admitted with serologically-confirmed dengue fever. He had been well until day 8 of illness, when he developed cerebellar signs and symptoms. The temporal relationship with the recent dengue fever suggested that he had dengue cerebellitis. He recovered well, with no neurological sequelae upon our clinic visit. CONCLUSIONS Dengue cerebellitis is a rare but recognized manifestation, which should be considered in patients from endemic areas of dengue fever who develop cerebellar syndrome.
  2. Khoo CS, Ramachandram S
    Malays J Med Sci, 2022 Dec;29(6):146-157.
    PMID: 36818902 DOI: 10.21315/mjms2022.29.6.14
    BACKGROUND: Children with autism spectrum disorder (ASD) are susceptible to excessive electronic screen media (ESM) use. This study aimed to evaluate the effectiveness of a parent training programme in improving the screen time and social functioning of children with ASD.

    METHODS: This pre-/post-test quasi-experimental study involved parents by providing them with structured education based on the American Academy of Pediatrics (AAP)' screen time recommendations. In total, 259 children with ASD aged 3 years old-12 years old were eligible. Of those children, 26 were excluded due to comorbidities or taking medications. Additionally, 28 parents participated. Children's screen time were recorded, and social behaviour was scored using the Social Responsiveness Scale pre- and post-intervention.

    RESULTS: There were significant reductions in the average daily screen time of children with ASD after their parents attended the training programme (-51.25 min; 95% CI: -78.40, -24.10). In subgroups with reduced screen time, the treatment effect of the intervention was significant in improving the social responsiveness total score (-3.09; 95% CI: -5.96, -0.22), the social communication scale (-3.64; 95% CI: -5.91, -1.36) and the restricted interest and repetitive behaviour (RRB) scale (-5.27; 95% CI: -10.29, -0.25).

    CONCLUSION: Parental training is effective in reducing screen time and improving social functioning in children with ASD.

  3. Arifin NM, Khoo CS
    Neurol Clin Pract, 2019 Feb;9(1):e10.
    PMID: 30859015 DOI: 10.1212/CPJ.0000000000000558
  4. Khoo CS, Ab Rahman SS
    Med J Aust, 2017 11 20;207(10):421.
    PMID: 29129168
  5. Khoo CS, Tan HJ, Sharis Osman S
    Am J Case Rep, 2018 Jul 13;19:825-828.
    PMID: 30002360 DOI: 10.12659/AJCR.909883
    BACKGROUND Dermal fillers are increasingly used for medical and aesthetic purposes in clinical practice. Common complications following filler injections include bruising, itching, infections, allergic reactions, and tissue necrosis. This case is the first report of Herpes simplex virus type 1 (HSV-1) encephalitis as a possible complication of dermal filler injection. CASE REPORT A 27-year-old woman with no past medical history presented with altered mental state, headaches, and seizures. She had a nasal dermal filler injection for aesthetic purpose five weeks before her acute presentation. A diagnosis of HSV-1 encephalitis was made based on brain imaging with computed tomography and magnetic resonance imaging (MRI) findings that showed bilateral frontotemporal lobe hyperintensity. Analysis of her cerebrospinal fluid (CSF) confirmed the presence of HSV-1 DNA. Despite anti-viral treatment with acyclovir, she developed postencephalitic syndrome. CONCLUSIONS This case report highlights the possibility that among the complications of the use of cosmetic dermal fillers, the transmission of HSV-1 and the development of HSV-1 encephalitis should be recognized.
  6. Sahdi H, Rasit AH, Khoo CS, Bojeng A, Nur-Alyana BA
    Malays Orthop J, 2019 Jul;13(2):52-55.
    PMID: 31467654 DOI: 10.5704/MOJ.1907.011
    Congenital humeroradial synostosis can occur as an isolated clinical entity or as part of a syndrome. Bilateral elbow fixed flexion deformity is very incapacitating and challenging to treat. Here we present the case of a boy with fixed flexion deformity of both elbows due bilateral humeroradial synostosis. Other characteristic features of multiple synostoses syndrome were also present in this child, his elder brother and mother. We elected to improve the position of the right elbow by adapting the modified French osteotomy described by Bellemore et al.
  7. Tee TY, Khoo CS, Raymond AA, Syazarina SO
    Neurology, 2019 08 06;93(6):e626-e627.
    PMID: 31383811 DOI: 10.1212/WNL.0000000000007905
  8. Khoo CS, Tee TY, Tan HJ, Ali RA
    J Neurosci Rural Pract, 2019 4 20;10(2):324-326.
    PMID: 31001027 DOI: 10.4103/jnrp.jnrp_315_18
    We report a patient with end-stage renal disease on peritoneal dialysis, who developed encephalopathy after receiving a few doses of cefepime. He recovered clinically and electroencephalographically after having discontinued the culprit agent and undergone hemodialysis. This case highlights the importance of promptly recognizing this reversible encephalopathy, which can lead to the avoidance of unnecessary workup, reduce the length of hospital stay, and thereby improve the patients' outcome.
  9. Rybalko ON, Kaladze NN, Sukhareva IA, Khoo CS
    J Neurosci Rural Pract, 2019 Oct;10(4):700-702.
    PMID: 31831992 DOI: 10.1055/s-0039-1700599
    Valproic acid or valproate is a well-recognized potent teratogen. Antenatal exposure to this drug can cause fetal valproate syndrome (FVS), which is a constellation of distinctive dysmorphic features and congenital malformations. Despite an abundance of reports and registries about this syndrome, there is lack of information from Russia, in particular, the Republic of Crimea. We herein describe two cases of FVS from our registry.
  10. Ag Lamat MSN, Khoo CS, Shaaya F
    Acta Neurol Belg, 2020 Dec;120(6):1437-1438.
    PMID: 32643118 DOI: 10.1007/s13760-020-01438-8
  11. Hassan Basri M, Khoo CS, Che Hamzah J
    Acta Neurol Belg, 2021 Apr;121(2):573-574.
    PMID: 33068282 DOI: 10.1007/s13760-020-01519-8
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