Kauvery Hospital Successfully Treats Rare Movement Disorders
Chennai Tamil Nadu India NewsVoir Five-year-old girl child and 20-year-old male receive treatment for rare Movement Disorders Right medical intervention administered at the right time key for effective recovery Kauvery Hospital Chennai a unit of Kauvery Group of Hospitals a leading multispecialty healthcare chain in Tamil Nadu today announced successful treatments of rare Movement Disorders The first patient a girl from Bangladesh aged 5 was undergoing treatment for Myoclonic Epilepsy a type of seizure with sudden muscle spasm for the last 2 years As a result of this diagnosis she was treated with multiple anti-epileptic medications As she continued to have these clinical events in spite of treatment for epilepsy she was brought to Kauvery Hospital at Chennai for further diagnosis and treatment After careful and thorough observation the medical experts from Kauvery Hospital diagnosed that the girl was being mistakenly treated for fits whereas she was exhibiting a rare movement disorder called Hyperekplexia which is also called exaggerated startle reaction in which affected individuals have increased muscle tone hypertonia and exhibit the exaggerates startle reaction as a response to unexpected stimuli especially loud noises The child underwent a test called Video-EEG to prove that there was no epileptic basis for these abnormal clinical events This study captures the brain activity with synchronised video recording and so a time locked capture of these abnormal movements can be done This special study of the brain is used to distinguish seizures from other non-seizure problems The family of the patient was then informed of the proper diagnosis and reassured that this was not a seizure disorder The patient was administered appropriate medication unwanted antiepileptic drug were removed with good response Hyperekplexia is a rare genetic disorder In most cases it is inherited as an autosomal dominant trait but can also follow autosomal recessive or X-linked inheritance Mutations in some specific genes are associated with the condition It is most often present at birth and affects both males and females In some individuals as in this instance onset of the disorder may be delayed until adolescence or adulthood However many patients have a benign course with reduction in startle episodes as they grow up Genetic counselling is available for affected families The second patient a young adult aged 20 was undergoing treatment for seizures for almost 15 years for an involuntary movement that occurred especially when he woke from his sleep These movements were quite dramatic with flailing movements of the limbs but with preserved consciousness The patient was on multiple drugs for epilepsy A thorough understanding of his medical history and special testing using Video-EEG indicated that he was not suffering with seizures but that this was a rare disorder of the nervous system called Paroxysmal Non-Kinesogenic Dyskinesia PNKD that caused periods of involuntary movement like irregular shaking and writhing movements of the limbs The patient and family were counselled and most of the unwanted anti-epileptic medications that he was taking were stopped Dr Bhuvaneshwari Rajendran Senior Consultant Neurology and Neurophysiology Kauvery Hospital Both these syndromes are very rare and cannot be easily identified PNKD – Paroxysmal Non-Kinesogenic Dyskinesia is so rare that its prevalence rate is 1 in 5 million people while Hyperekplexia occurs for 1 in fifty thousand people When these patients presented to us we carefully studied their case history as they had features that were unique and were not consistent with the diagnosis of fits After a detailed clinical examination and after witnessing some of the episodes it was clear that these clinical events were not seizures We immediately organized Video-EEG Electroencephalography – a test that detects abnormalities in your brain waves or in the electrical activity of your brain to capture episodes and proved that these episodes did not have an epileptic basis It was very unfortunate that both these young patients were on the wrong medication for such long periods of time If left undiagnosed both these syndromes would have done more damage to their already troubled lives We are happy that we were able to identify the condition accurately and steer the patients recovery in the right direction These rare movement disorders are mostly mistaken for seizures and patients have very little understanding of these conditions At Kauvery Hospital we have clinical expertise and tools like Video-EEG Electroencephalography which is a very useful tool to distinguish seizures from non-Epileptic involuntary movements Such technology helps to diagnose such unusual disorders Advanced medical infrastructures and equipment pave way for better management and treatment of such patients I would like to congratulate DrBhuvaneshwari and her team for utilizing the state-of-the-art medical technologies available at our facility to identify such rare syndromes and help these patients towards their recovery said Dr Aravindan Selvaraj Co-founder and Executive Director Kauvery Hospital Chennai Both patients are responding well to the treatment and are recovering PWR PWR
Chennai Tamil Nadu India NewsVoir Five-year-old girl child and 20-year-old male receive treatment for rare Movement Disorders Right medical intervention administered at the right time key for effective recovery Kauvery Hospital Chennai a unit of Kauvery Group of Hospitals a leading multispecialty healthcare chain in Tamil Nadu today announced successful treatments of rare Movement Disorders The first patient a girl from Bangladesh aged 5 was undergoing treatment for Myoclonic Epilepsy a type of seizure with sudden muscle spasm for the last 2 years As a result of this diagnosis she was treated with multiple anti-epileptic medications As she continued to have these clinical events in spite of treatment for epilepsy she was brought to Kauvery Hospital at Chennai for further diagnosis and treatment After careful and thorough observation the medical experts from Kauvery Hospital diagnosed that the girl was being mistakenly treated for fits whereas she was exhibiting a rare movement disorder called Hyperekplexia which is also called exaggerated startle reaction in which affected individuals have increased muscle tone hypertonia and exhibit the exaggerates startle reaction as a response to unexpected stimuli especially loud noises The child underwent a test called Video-EEG to prove that there was no epileptic basis for these abnormal clinical events This study captures the brain activity with synchronised video recording and so a time locked capture of these abnormal movements can be done This special study of the brain is used to distinguish seizures from other non-seizure problems The family of the patient was then informed of the proper diagnosis and reassured that this was not a seizure disorder The patient was administered appropriate medication unwanted antiepileptic drug were removed with good response Hyperekplexia is a rare genetic disorder In most cases it is inherited as an autosomal dominant trait but can also follow autosomal recessive or X-linked inheritance Mutations in some specific genes are associated with the condition It is most often present at birth and affects both males and females In some individuals as in this instance onset of the disorder may be delayed until adolescence or adulthood However many patients have a benign course with reduction in startle episodes as they grow up Genetic counselling is available for affected families The second patient a young adult aged 20 was undergoing treatment for seizures for almost 15 years for an involuntary movement that occurred especially when he woke from his sleep These movements were quite dramatic with flailing movements of the limbs but with preserved consciousness The patient was on multiple drugs for epilepsy A thorough understanding of his medical history and special testing using Video-EEG indicated that he was not suffering with seizures but that this was a rare disorder of the nervous system called Paroxysmal Non-Kinesogenic Dyskinesia PNKD that caused periods of involuntary movement like irregular shaking and writhing movements of the limbs The patient and family were counselled and most of the unwanted anti-epileptic medications that he was taking were stopped Dr Bhuvaneshwari Rajendran Senior Consultant Neurology and Neurophysiology Kauvery Hospital Both these syndromes are very rare and cannot be easily identified PNKD – Paroxysmal Non-Kinesogenic Dyskinesia is so rare that its prevalence rate is 1 in 5 million people while Hyperekplexia occurs for 1 in fifty thousand people When these patients presented to us we carefully studied their case history as they had features that were unique and were not consistent with the diagnosis of fits After a detailed clinical examination and after witnessing some of the episodes it was clear that these clinical events were not seizures We immediately organized Video-EEG Electroencephalography – a test that detects abnormalities in your brain waves or in the electrical activity of your brain to capture episodes and proved that these episodes did not have an epileptic basis It was very unfortunate that both these young patients were on the wrong medication for such long periods of time If left undiagnosed both these syndromes would have done more damage to their already troubled lives We are happy that we were able to identify the condition accurately and steer the patients recovery in the right direction These rare movement disorders are mostly mistaken for seizures and patients have very little understanding of these conditions At Kauvery Hospital we have clinical expertise and tools like Video-EEG Electroencephalography which is a very useful tool to distinguish seizures from non-Epileptic involuntary movements Such technology helps to diagnose such unusual disorders Advanced medical infrastructures and equipment pave way for better management and treatment of such patients I would like to congratulate DrBhuvaneshwari and her team for utilizing the state-of-the-art medical technologies available at our facility to identify such rare syndromes and help these patients towards their recovery said Dr Aravindan Selvaraj Co-founder and Executive Director Kauvery Hospital Chennai Both patients are responding well to the treatment and are recovering PWR PWR
