All Relations between Dysarthria and Diplopia

Publication Sentence Publish Date Extraction Date Species
Luca Gregorio Giaccari, Donatella Mastria, Rosella Barbieri, Rossella De Maglio, Francesca Madaro, Gianfranco Paiano, Maria Caterina Pace, Pasquale Sansone, Giuseppe Pulito, Luciana Masci. Bickerstaff encephalitis in childhood: a review of 74 cases in the literature from 1951 to today. Frontiers in neurology. vol 15. 2024-03-27. PMID:38533411. the most frequent initial symptoms were consciousness disturbance, headache, vomiting, diplopia, gait disturbance, dysarthria and fever. 2024-03-27 2024-03-29 Not clear
Larisa Cujba, Ovidiu Samoila, Silvina Ilut, Vitalie Vacaras, Cristina Sta. The key role of the ophthalmologist in diagnosing botulism: two case reports. Germs. vol 12. issue 4. 2023-12-01. PMID:38021184. botulinum toxin, the strongest known neurotoxin, is the cause of a rare fatal neuroparalytic disease characterized by the so-called "four ds": diplopia, dysarthria, dysphagia, dry mouth. 2023-12-01 2023-12-07 Not clear
Larisa Cujba, Ovidiu Samoila, Silvina Ilut, Vitalie Vacaras, Cristina Sta. The key role of the ophthalmologist in diagnosing botulism: two case reports. Germs. vol 12. issue 4. 2023-12-01. PMID:38021184. botulinum toxin, the strongest known neurotoxin, is the cause of a rare fatal neuroparalytic disease characterized by the so-called "four ds": diplopia, dysarthria, dysphagia, dry mouth. 2023-11-29 2023-12-07 Not clear
Hagy Hannah, Gianna Hill, Maureen Lac. A - 49 Neuropsychological and Clinical Features of Ataxia Due to CACNA1A (P.1661H) Mutation: a Case Study. Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists. 2023-10-09. PMID:37807145. on the other hand, cacna1a mutation with specific protein variant r1661h involvement is associated with ea2, characterized by early onset ataxia, which may be accompanied by vertigo, diplopia, dysarthria, and generalized weakness. 2023-10-09 2023-10-15 Not clear
Annibale Antonioni, Vittorio Rispoli, Patrik Fazio, Nico Golfrè Andreasi, Vittorio Govoni, Enrico Granier. Development of Parkinsonism in a Patient with Central Pontine Myelinolysis. Neurology international. vol 14. issue 3. 2022-09-22. PMID:36135990. it generally manifests with acute paraparesis/tetraparesis, dysphagia, dysarthria, diplopia, and loss of consciousness, as well as hallucinations, spasms, and other neurological symptoms related to brainstem damage. 2022-09-22 2023-08-14 Not clear
Mustafa Al-Chalabi, Nicholas R DelCimmuto, Azizullah Beran, Pratyush Pavan Devarasetty, Asmaa Mhanna, Naeem Mahfooz, Ajaz Sheik. Clinical characteristics, management, and outcomes of CLIPPERS: A comprehensive systematic review of 140 patients from 100 studies. Multiple sclerosis and related disorders. vol 68. 2022-08-27. PMID:36029706. chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (clippers) is a rare inflammatory disorder of the central nervous system, characterized by symptoms referable to the brainstem and cerebellum such as, diplopia, gait ataxia and cerebellar dysarthria. 2022-08-27 2023-08-14 Not clear
Nik Mohamed Firdaus Nik Mohamed Kamal, Nasibah Mohamad, Bazli Md Yusof. Dizziness and syncope after subclavian steal: A case report of a rarely symptomatic, common vascular disorder. Malaysian family physician : the official journal of the Academy of Family Physicians of Malaysia. vol 17. issue 1. 2022-04-20. PMID:35440963. nevertheless, some patients may present with arm ischemia or signs and symptoms of vertebrobasilar insufficiency, such as vertigo, dizziness, diplopia, ataxia, dysarthria, and syncopal episodes. 2022-04-20 2023-08-13 Not clear
Yelena Shames, Mimma Errante, Nana Prempeh Ketek. Myasthenia Gravis: A Rare Neurologic Complication of Immune Checkpoint Inhibitor Therapy. Journal of the advanced practitioner in oncology. vol 13. issue 2. 2022-04-04. PMID:35369395. ocular, respiratory, bulbar, and skeletal muscles are most commonly affected; therefore, patients often present with fatigable ptosis, blurry vision, diplopia, change in facial expression, dysphagia, dysarthria, dyspnea, and limb weakness. 2022-04-04 2023-08-13 Not clear
Aaron S Bower, Adeniyi Fisayo, Joachim M Baehring, Bhaskar Ro. Clinical Reasoning: A 73-Year-Old Woman With Episodic Dysarthria and Horizontal Binocular Diplopia. Neurology. 2022-03-10. PMID:35264421. clinical reasoning: a 73-year-old woman with episodic dysarthria and horizontal binocular diplopia. 2022-03-10 2023-08-13 Not clear
Maria A Tuna, Peter M Rothwel. Diagnosis of non-consensus transient ischaemic attacks with focal, negative, and non-progressive symptoms: population-based validation by investigation and prognosis. Lancet (London, England). vol 397. issue 10277. 2021-11-04. PMID:33676629. there is consensus on classic symptoms (eg, motor weakness, dysphasia, hemianopia, monocular visual loss) but no consensus on several monosymptomatic events with sudden-onset, non-progressive, focal negative symptoms (eg, isolated diplopia, dysarthria, vertigo, ataxia, sensory loss, and bilateral visual disturbance), with much variation in investigation and treatment. 2021-11-04 2023-08-13 Not clear
Oscar O Gasca-González, Julio C Pérez-Cruz, Matias Baldoncini, Mario A Macías-Duvignau, Luis Delgado-Reye. Neuroanatomical basis of Wallenberg syndrome. Cirugia y cirujanos. vol 88. issue 3. 2021-05-17. PMID:32539005. its signs and symptoms include vertigo, nystagmus, diplopia, ipsilateral horner syndrome, facial ruddiness and dry skin, dysphonia, dysphagia, dysarthria, ipsilateral loss of gag reflex, ipsilateral ataxia, ipsilateral impaired taste, ipsilateral facial pain and paresthesia, decreased ipsilateral blink reflex, contralateral hypoalgesia and thermoanaesthesia in the trunk and limbs; and ipsilateral facial hypoalgesia and thermoanaesthesia. 2021-05-17 2023-08-13 Not clear
Domenico Chirchiglia, Pasquale Chirchiglia, Rosa Marott. A singular association of migraine with brainstem aura and Alice in Wonderland syndrome. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 35. issue 8. 2020-11-10. PMID:31049666. in this work, we describe an association of brainstem headache with aura (bha) and alice in wonderland syndrome (aiws) in a 17-year-old male, suffering from crises of vertigo, weakness, dysarthria, and diplopia, in half-hour duration, followed by diffuse or occipital headache, lasting several hours. 2020-11-10 2023-08-13 Not clear
Devin E Prior, Vijay Reng. Comparison of costs and outcomes of patients presenting with a rare brainstem syndrome. eNeurologicalSci. vol 13. 2020-10-01. PMID:30450430. in this case report we compare two patients presenting with similar symptoms of a brainstem syndrome including ataxia, dysarthria, and diplopia. 2020-10-01 2023-08-13 Not clear
Enrico Ferrante, Maria Raffaella Marazzi, Michele Trimboli, Davide Dalla Costa, Cristina Erminio, Lino Nobil. Brainstem lesion causing paroxysmal ataxia, dysarthria, diplopia and hemifacial spasm (PADDHS). Epileptic disorders : international epilepsy journal with videotape. vol 21. issue 4. 2020-03-27. PMID:31371274. brainstem lesion causing paroxysmal ataxia, dysarthria, diplopia and hemifacial spasm (paddhs). 2020-03-27 2023-08-13 Not clear
Geneviève Demarquay, Anne Ducros, Alexandra Montavont, François Mauguier. Migraine with brainstem aura: Why not a cortical origin? Cephalalgia : an international journal of headache. vol 38. issue 10. 2019-01-25. PMID:29073774. background migraine with brainstem aura is defined as a migraine with aura including at least two of the following symptoms: dysarthria, vertigo, tinnitus, hypacusis, diplopia, ataxia and/or decreased level of consciousness. 2019-01-25 2023-08-13 Not clear
Jean Paul Bouwyn, Patrick Magnier, Anne-Laure Bédat-Millet, Patrick Ahtoy, David Maltête, Romain Lefaucheu. Anti-MuSK myasthenia gravis with prolonged remission. Neuromuscular disorders : NMD. vol 26. issue 7. 2018-01-24. PMID:27161384. we report the case of a 22-year-old man who presented with diplopia on lateral gaze to both sides, facial diplegia, nasal dysarthria and dysphagia. 2018-01-24 2023-08-13 Not clear
Philippa C Lavallée, Leila Sissani, Julien Labreuche, Elena Meseguer, Lucie Cabrejo, Céline Guidoux, Isabelle F Klein, Pierre-Jean Touboul, Pierre Amarenc. Clinical Significance of Isolated Atypical Transient Symptoms in a Cohort With Transient Ischemic Attack. Stroke. vol 48. issue 6. 2017-07-19. PMID:28487336. contrary to typical transient symptoms (ts), atypical ts, such as partial sensory deficit, dysarthria, vertigo/unsteadiness, unusual cortical visual deficit, and diplopia, are not usually classified as symptoms of transient ischemic attack when they occur in isolation, and their clinical relevance is frequently denied. 2017-07-19 2023-08-13 Not clear
Aubree Bruhnding, Derek Notch, Albertine Bear. Anti-Yo positive paraneoplastic cerebellar degeneration in the setting of cholangiocarcinoma. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 36. 2017-02-06. PMID:27816258. subacute cerebellar ataxia, or paraneoplastic cerebellar degeneration, usually presents in women with a subcate onset of gait instability, followed by progressive limb and trunk ataxia, dysarthria, diplopia, and dysphagia that occurs in the setting of, or precedes the diagnosis of, a gynecologic or breast malignancy and clinically stabilizes within six months. 2017-02-06 2023-08-13 Not clear
Ching-Fu Weng, Ding-Cheng Chan, Ya-Fang Chen, Fei-Chih Liu, Horng-Huei Lio. Chronic hepatitis B infection presenting with chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): a case report. Journal of medical case reports. vol 9. 2016-06-27. PMID:26582039. chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids is a brainstem disorder characterized by perivascular pathologic reaction with lymphocyte infiltration and leading to diplopia, facial palsy, dysarthria, and gait ataxia. 2016-06-27 2023-08-13 Not clear
Gaurav M Kasundra, Amita Narendra Bhargava, Bharat Bhushan, Khichar Shubhakaran, Isha Soo. Polyneuritis cranialis with generalized hyperreflexia as a presenting manifestation of thyrotoxicosis. Annals of Indian Academy of Neurology. vol 18. issue 2. 2015-05-28. PMID:26019429. a 22-year-old male student with no past medical illness, presented with acute onset dysarthria, binocular diplopia, and dysphagia over 10 hours. 2015-05-28 2023-08-13 Not clear