Publications by authors named "M Moodley"

Infections by non-O1/non-O139 serogroups of Vibrio cholerae (NOVC) are increasing worldwide. Infected patients usually display self-limiting diarrhoea or external ear and wound infections. We present a rare case of bacteraemia secondary to NOVC infection.

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Article Synopsis
  • - Neurofibromatosis type 2-related schwannomatosis (NF2-SWN) is a genetic disorder caused by mutations in the NF2 gene, affecting about 1 in 50,000 people globally, leading to the development of various tumors in the central nervous system.
  • - The condition is characterized by the occurrence of bilateral vestibular schwannomas in over 95% of patients, along with other tumors such as meningiomas and gliomas, as well as potential eye issues.
  • - Early detection through thorough medical exams is crucial for managing NF2-SWN, and most patients benefit from a combination of treatments, including surgery.
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Neurofibromatosis type 1 (NF1) is one of the most common genetic conditions. It can be inherited in an autosomal dominant manner, but almost half of cases occur de novo. NF1 is associated with café-au-lait macules, freckles in the inguinal and axillary region, neurofibromas, Lisch nodules of the iris or choroidal abnormalities, optic pathway gliomas, and distinctive bone anomalies.

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Objectives: Clostridioides difficile infection is a serious healthcare-associated infection linked to antimicrobial use. The severity of the disease can be associated with hypervirulent ribotypes such as RT027. The study aimed to investigate the molecular epidemiology and genomic characteristics of C.

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Background: Isolated psychiatric symptoms can be the initial symptom of pediatric anti-N-methyl-d-aspartate (NMDA) receptor autoimmune encephalitis (pNMDARE). Here we report on the prevalence of isolated psychiatric symptoms in pNMDARE. We also assess whether initial neurodiagnostic tests (brain magnetic resonance imaging [MRI], electroencephalography [EEG], and/or cerebrospinal fluid [CSF] white blood cell count) are abnormal in children with isolated psychiatric symptoms and pNMDARE.

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