Displaying all 6 publications

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  1. Chew NK, Sim BF, Tan CT, Goh KJ, Ramli N, Umapathi P
    Neurology, 2001 Aug 14;57(3):529-31.
    PMID: 11502928
    In a hospital series of 70 patients on follow-up after radiotherapy for nasopharyngeal carcinoma, 14 patients (20%) developed delayed post-irradiation bulbar palsy 1 to 18 years after radiotherapy (mean 5.5 years). Functional disability was moderate to severe. Three patients had aspiration pneumonia with one mortality. Post-irradiation bulbar palsy was a common complication and probably resulted from direct neuronal damage.
    Matched MeSH terms: Bulbar Palsy, Progressive/etiology*; Bulbar Palsy, Progressive/physiopathology
  2. Hamidon BB
    Med J Malaysia, 2006 Jun;61(2):245-7.
    PMID: 16898323 MyJurnal
    Acute Guillain-Barre syndrome (GBS) is characterized by an acute onset of limb weakness and areflexia. There are a few rare variants that have been described and one of them is the pharyngeal-cervical-brachial (PCB) variant (oropharynx, neck, and proximal upper limb muscles). However, in this patient, the only presentation was bulbar involvement with fast recovery within days. This is likely to be the milder form of PCB that has rarely been described before. A 19-year-old Malay lady presented with progressive dysphagia associated with nasal voice for one week duration. There was no limb weakness. Examination showed generalized areflexia. Pharyngeal and palatal muscles were markedly weak. Cerebrospinal fluid (CSF) examination showed raised protein level. Nerve conduction studies revealed generalized demyelinating motor polyneuropathy consistent with GBS. The patient fully recovered within three days and was discharged well.
    Matched MeSH terms: Bulbar Palsy, Progressive/complications; Bulbar Palsy, Progressive/diagnosis*
  3. Tan JSH, Lee S, Hiew FL
    eNeurologicalSci, 2021 Mar;22:100321.
    PMID: 33553704 DOI: 10.1016/j.ensci.2021.100321
    Amyotrophic lateral sclerosis (ALS) is characterized by progressive onset motor deficits with heterogenous presentations ranging from dysarthria to foot drop. Approximately 20% of the patients present with focal bulbar symptoms, in which some may remain restricted to bulbar region (isolated bulbar palsy), and the remaining eventually spreads to involve other body regions (classical ALS). Without accompanying upper and lower motor neurons signs elsewhere, differential diagnoses for isolated bulbar symptoms are extensive, include ALS variants as well as potentially treatable mimics. Therefore, it is important to take heed on every possible aetiology that may disrupt the hypoglossal nucleus, nerve, or lingual muscle itself. Herein, we illustrated a rare presentation of Group A basilar invagination, which mimicked bulbar-onset ALS.
    Matched MeSH terms: Bulbar Palsy, Progressive
  4. Lau KF, Tan KS, Goh KJ, Ramli N, Tai SM
    Ann Acad Med Singap, 2019 Mar;48(3):109-111.
    PMID: 30997481
    Matched MeSH terms: Bulbar Palsy, Progressive/etiology
  5. Ong SG, Ding HJ
    Int J Rheum Dis, 2017 Dec;20(12):2175-2178.
    PMID: 26692320 DOI: 10.1111/1756-185X.12814
    Matched MeSH terms: Bulbar Palsy, Progressive/chemically induced*; Bulbar Palsy, Progressive/diagnosis; Bulbar Palsy, Progressive/drug therapy; Bulbar Palsy, Progressive/immunology
  6. Tay CH, Jek WT
    Med J Malaya, 1972 Jun;26(4):272-7.
    PMID: 5069417
    Matched MeSH terms: Bulbar Palsy, Progressive
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