Progressive Bulbar Palsy (PBP) or Bulbar Onset MND: “A Case Report”
A patient with enhancing bulbar palsy, a type of efferent neuron disease that causes hypertrophy and twitching of the tongue’s musculature, dysphagia, dysarthria, and an excessive buildup of secretions, is described.
Sagar S. Bhovare, Akhataribano S. Sayyad
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Palliative Care Challenges of Patients With Progressive Bulbar Palsy: A Retrospective Case Series of 14 Patients [PDF]
Progressive bulbar palsy (PBP) is a form of motoneuron disease and is widely classified as a subtype of amyotrophic lateral sclerosis (ALS) with a shorter time of survival and female predominance. In this retrospective case series of 14 patients with PBP,
Sarah K. Bublitz +8 more
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A case report on Ayurvedic management of progressive bulbar palsy-A rare amyotrophic lateral sclerosis phenotype [PDF]
This case report is the description of a devastating illness, Progressive Bulbar Palsy (PBP) of a sixty-seven years old male patient. He presented with complaints of slurred speech, hearing impairment, generalised weakness of limbs, weakened grip to hold
Sinimol Thekkekkoottumughath Peethambaran +2 more
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Creativity and Mental Illness: A Case Study of a Patient with Progressive Bulbar Palsy
Creativity and the production of artwork can have an impact on the course and treatment of comorbid severe mental illness and neurodegeneration. We report on a 70-year-old male patient with highly original artistic behavior, who suffered from lifelong ...
Felix Geser +5 more
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Neuro-Behçet’s masquerading as progressive bulbar palsy: a case report and literature review [PDF]
In patients with progressive bulbar palsy without an obvious cause, there should be a high index of suspicion for the potential diagnosis of Neuro-Behçet’s Disease, even in the absence of the acute classical peripheral manifestations of Bechet’s Disease,
Theodoros Paschalis +3 more
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an adult-onset inherited small vessel disease of the brain caused by NOTCH3 mutations.
Elif GÖKÇAL +3 more
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Gelsolin variant amyloidosis mimicking progressive bulbar palsy
Hereditary gelsolin amyloidosis, a rare autosomal dominant hereditary disease, is caused by pathogenic variants in the gelsolin ( GSN ) gene. 1 It is characterized by slowly progressive cranial and peripheral nerve degeneration, corneal lattice dystrophy,
Jinseok Park +6 more
semanticscholar +3 more sources
Injury of the arcuate fasciculus in a patient with progressive bulbar palsy
Min Cheol Chang +2 more
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An Atypical Descending Variant of Guillain-Barré Syndrome With Bulbar Palsy, Autonomic Instability, and Delayed Colonic Pseudo-Obstruction: A Case Report. [PDF]
Guillain-Barré syndrome (GBS) is an acute, immune-mediated polyradiculoneuropathy that is the most common cause of acute flaccid paralysis worldwide. The classical form manifests as an ascending, symmetrical weakness, but atypical variants, including ...
Sahu TA.
europepmc +2 more sources

