scholarly journals Benign fasciculations and Corticosteroid use: possible association? An update

2011 ◽  
Vol 3 (2) ◽  
pp. 11 ◽  
Author(s):  
Marco Orsini ◽  
Flavio R. Sztajnbok ◽  
Acary Bulle Oliveira ◽  
Marco Antonio Araújo Leite ◽  
Peter Salem Júnior ◽  
...  

Fasciculations are characterized by visible subtle and fast contractions of muscle, even wormlike in movement, by the contraction of a fascicle of muscle fibers. The authors present the case study of a 28-year-old patient with the appearance of migratory and diffuse fasciculations with an onset after partial tapering off of oral corticosteroides (60 mg total dose) indicated for treatment of Minimal change Glomerulopathy. Clinical Neurological physical exam allied with an ENMG, besides other complementary laboratory exams were used for screening the above-mentioned patient. Afterwards, current research relating to the topic at hand was made in order to update the data available in the Bireme, Scielo and PubMed Data Banks using the following key words: Fasciculation’s, motor neuron disease, and benign fasciculations in the Portuguese, English as well as Spanish language. Although fasciculation’s are most commonly associated with Motor neuron disease as well as with certain metabolic disorders, they may also be present in individuals with absolutely no underlying pathological disorders. In our case, fasciculation potentials that have been present for six months, with no other signs of a neurogenic disorder as well as absence of laboratory findings, the patient received a diagnosis of Benign Fasciculation Syndrome (BFS).We believe that the use of corticosteroides in high doses with subsequent tapering contributed to the fasciculation’s, especially due to the changes that this causes on the ionic channels. Fasciculation’s are symptoms seen in a large range of conditions, and also being the main symptom of the so-called Benign Fasciculation Syndrome. We have presented an example of this clinical syndrome in a patient whose complaint was fasciculation’s, with complete clinical remission of symptoms following complete tapering off of corticosteroid six months previously.

2021 ◽  
Vol 7 (1) ◽  
pp. 13-18
Author(s):  
TU Ebin ◽  
◽  
PTN Vasudevan Moos ◽  
AN Nambi ◽  
◽  
...  

Motor-neuron disease (MND) is a neuro-degenerative disease characterized by muscle wasting and loss of muscle strength. Amyotrophic lateral sclerosis (ALS) is the commonest among MND. Bibrachial amyotrophic diplegia is a variant of ALS where the disease is restricted to upper limbs. A case of Bibrachial amyotophy charaterised by weakness of both upper limbs associated with wasting was managed in SNA Ayurveda Nursing home. The condition is considered as Vataroga with special designation as ‘Bahusosha’. A 21 days treatment course was planned and executed which include Snehana, Swedana, Sodhana and Rasayana chikitsa. The patient was assessed symptomatically. A weekly assessment based on the quality of his daily activities was performed. A satisfactory improvement was observed with gradual gaining of upper limb strength. There was betterment in his gross and fine motor activities including quality of writing. The principle line of treatment was Dosha vilayana, Dosha sodhana, and Dathu vardhana which is found to be suitable for Vata – Kapha Roga.


1986 ◽  
Vol 19 (6) ◽  
pp. 568-572 ◽  
Author(s):  
Neil R. Cashman ◽  
Jack P. Antel ◽  
Larry W. Hancock ◽  
Glyn Dawson ◽  
Allen L. Horwitz ◽  
...  

2017 ◽  
Vol 41 (2) ◽  
pp. 328
Author(s):  
Hyeonjun Oh ◽  
Seong Woong Kang ◽  
Won Ah Choi ◽  
Jang Woo Lee ◽  
Miri Suh ◽  
...  

2021 ◽  
Vol 8 (2) ◽  
pp. e962
Author(s):  
Jana Werner ◽  
Ilijas Jelcic ◽  
Esther Irene Schwarz ◽  
Elisabeth Probst-Müller ◽  
Jakob Nilsson ◽  
...  

ObjectiveTo expand the spectrum of anti-IgLON5 disease by adding 5 novel anti-IgLON5–seropositive cases with bulbar motor neuron disease-like phenotype.MethodsWe characterized the clinical course, brain MRI and laboratory findings, and therapy response in these 5 patients.ResultsPatients were severely affected by bulbar impairment and its respiratory consequences. Sleep-related breathing disorders and parasomnias were common. All patients showed clinical or electrophysiologic signs of motor neuron disease without fulfilling the diagnostic criteria for amyotrophic lateral sclerosis. One patient regained autonomy in swallowing and eating, possibly related to immunotherapy.ConclusionIgLON5 disease is an important differential diagnosis to evaluate in patients with bulbar motor neuron disease-like phenotype and sleep disorders. There is need for a deeper understanding of the underlying pathobiology to determine whether IgLON5 disease is an immunotherapy-responsive condition.


Author(s):  
Giulia Bisogni ◽  
Angela Romano ◽  
Amelia Conte ◽  
Giorgio Tasca ◽  
Daniela Bernardo ◽  
...  

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