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Resistant Tremors and Unexplained Weight Loss Could Also Be a Sign of HIV
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作者 Mohammed Hamdy Ibrahim shivram kumar +2 位作者 Janhavi Sirsat Mohamed Khalid Kiran kumar 《Neuroscience & Medicine》 2015年第3期81-83,共3页
This case study is done to show a different type of presentation of a HIV (Human Immunodeficiency Virus) patient. Neurological symptoms in HIV are normally due to Progressive Multifocal Leukoencephalopathy (PML) which... This case study is done to show a different type of presentation of a HIV (Human Immunodeficiency Virus) patient. Neurological symptoms in HIV are normally due to Progressive Multifocal Leukoencephalopathy (PML) which is a reactivated infection caused by John Cunningham virus (JC virus). The disease causes fatal demyelination of the central nervous system (CNS). This case presented a 51-year-old Nigerian man who complained of resistant tremors and unexplained weight loss. The patient was suspected to have HIV when a MRI scan revealed T2/FLAIR hyper intensity of white matter which was a sign of PML. HIV ELISA was done and came back with a positive result. PML presenting in the form of tremors is very rare and more research is required to focus on the neurological presentation of HIV. 展开更多
关键词 Human IMMUNODEFICIENCY Virus Tremors Progressive MULTIFOCAL LEUKOENCEPHALOPATHY
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Could Dystonia Be Initial Presentation of Corpus Callosum Infarction in Young Age Patients? A Case Report Study
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作者 Mohamed Hamdy Ibrahim Alyaa Fadhil +5 位作者 Sameh Saied Ali Salma Fathy Abdel Kader Mohamed Khalid Kiran kumar shivram kumar Janhavi Sirsat 《Neuroscience & Medicine》 2015年第2期62-64,共3页
Focal dystonia in young aged patients is considered to be the uncommon clinical presentation, unless a secondary cause is to be considered. Infarcts of the corpus callosum are rare and have not been well documented pr... Focal dystonia in young aged patients is considered to be the uncommon clinical presentation, unless a secondary cause is to be considered. Infarcts of the corpus callosum are rare and have not been well documented previously. As for a variety of signs and symptoms due to corpus callosum lesion, focal dystonia can be easily overlooked. The case is approved by ethical committee and explained to the patient with patient approval. 展开更多
关键词 FOCAL DYSTONIA CORPUS Callosum INFARCTION Involuntary Movement
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Case Report on Epilepsy with Cough Aura
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作者 Mohamed Hamdy Ibrahim Ahmed El Mansory +1 位作者 shivram kumar Janhavi Sirsat 《Neuroscience & Medicine》 2015年第1期1-4,共4页
The case study is aimed at providing a more thorough analysis of a case of Epilepsy presented with an unusual aura of cough. The study hopes to generate an interest for further studies into the topic and focuses on ab... The case study is aimed at providing a more thorough analysis of a case of Epilepsy presented with an unusual aura of cough. The study hopes to generate an interest for further studies into the topic and focuses on abnormal unusual presentations of auras. Cough as an aura is not a common presentation. Any stereotyped repeated clinical phenomenon should consider being epileptic in its origin. 展开更多
关键词 EPILEPSY COUGH AURA CHRONIC BRONCHITIS
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Case Report on Hiccup and Lateral Medullary Syndrome
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作者 Mohamed Hamdy Ibrahim Alyaa Fadhil +5 位作者 Sameh Saied Ali Salma Fathy Abdel Kader Mohamed Khalid Kiran kumar shivram kumar Janhavi Sirsat 《Neuroscience & Medicine》 2015年第2期58-61,共4页
The case study is aimed at providing a more thorough analysis of a case of lateral medullary syn-drome presented only with persistent hiccup after eating lunch the study hopes to generate an interest for further studi... The case study is aimed at providing a more thorough analysis of a case of lateral medullary syn-drome presented only with persistent hiccup after eating lunch the study hopes to generate an interest for further studies into the topic and focuses on abnormal unusual presentations of lateral medullary syndrome. Ethical committee has approved this case after taking consent from the patient and explaining to him the importance of the case in clinical practice. 展开更多
关键词 HICCUP LATERAL MEDULLARY SYNDROME STROKE
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