Child Neurology Board Prep podcast

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المحتوى المقدم من Roshan Srinivasan, MD and MD. يتم تحميل جميع محتويات البودكاست بما في ذلك الحلقات والرسومات وأوصاف البودكاست وتقديمها مباشرة بواسطة Roshan Srinivasan, MD and MD أو شريك منصة البودكاست الخاص بهم. إذا كنت تعتقد أن شخصًا ما يستخدم عملك المحمي بحقوق الطبع والنشر دون إذنك، فيمكنك اتباع العملية الموضحة هنا https://ar.player.fm/legal.

In Her Ellement

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Navigating Career Pivots and Grit with Milo’s Avni Patel Thompson 26:18

منذ 26 يومًا26:18

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How do you know when it’s time to make your next big career move? With International Women’s Day around the corner, we are excited to feature Avni Patel Thompson, Founder and CEO of Milo. Avni is building technology that directly supports the often overlooked emotional and logistical labor that falls on parents—especially women. Milo is an AI assistant designed to help families manage that invisible load more efficiently. In this episode, Avni shares her journey from studying chemistry to holding leadership roles at global brands like Adidas and Starbucks, to launching her own ventures. She discusses how she approaches career transitions, the importance of unpleasant experiences, and why she’s focused on making everyday life easier for parents. [01:26] Avni's University Days and Early Career [04:36] Non-Linear Career Paths [05:16] Pursuing Steep Learning Curves [11:51] Entrepreneurship and Safety Nets [15:22] Lived Experiences and Milo [19:55] Avni’s In Her Ellement Moment [20:03] Reflections Links: Avni Patel Thompson on LinkedIn Suchi Srinivasan on LinkedIn Kamila Rakhimova on LinkedIn Ipsos report on the future of parenting About In Her Ellement: In Her Ellement highlights the women and allies leading the charge in digital, business, and technology innovation. Through engaging conversations, the podcast explores their journeys—celebrating successes and acknowledging the balance between work and family. Most importantly, it asks: when was the moment you realized you hadn’t just arrived—you were truly in your element? About The Hosts: Suchi Srinivasan is an expert in AI and digital transformation. Originally from India, her career includes roles at trailblazing organizations like Bell Labs and Microsoft. In 2011, she co-founded the Cleanweb Hackathon, a global initiative driving IT-powered climate solutions with over 10,000 members across 25+ countries. She also advises Women in Cloud, aiming to create $1B in economic opportunities for women entrepreneurs by 2030. Kamila Rakhimova is a fintech leader whose journey took her from Tajikistan to the U.S., where she built a career on her own terms. Leveraging her English proficiency and international relations expertise, she discovered the power of microfinance and moved to the U.S., eventually leading Amazon's Alexa Fund to support underrepresented founders. Subscribe to In Her Ellement on your podcast app of choice to hear meaningful conversations with women in digital, business, and technology.…

Child Neurology Board Prep

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🎙 Child Neurology Board Prep is your go-to podcast for high-yield pediatric neurology review. Designed for residents, fellows, and practicing neurologists preparing for the boards, each episode breaks down essential topics in a concise, easy-to-digest format. From epilepsy and metabolic disorders to neurogenetics and neuromuscular conditions, we cover key concepts, case-based discussions, and board-style questions to help you solidify your knowledge. Whether you're commuting, working out, or taking a quick study break, tune in to sharpen your skills and stay board-ready! 🔬 Hosted by BrainSparks,MD

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Child Neurology Board Prep

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Child Neurology Board Prep

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Part 10: Pediatric Epilepsy Board Prep Q&A 12:42

منذ 16 hours12:42

12:42

S ummary This podcast episode covers various cases in child neurology, focusing on different types of seizures, their diagnosis, management, and implications, especially in special populations like pregnant women. The discussion includes psychogenic non-epileptic seizures, language regression in children, the impact of anti-seizure medications during pregnancy, and urgent treatment protocols for status epilepticus. The episode also addresses genetic factors in epilepsy, the ketogenic diet for specific conditions, and the importance of timely diagnostics in cases of syncope and seizure disorders. T akeaways Psychogenic non-epileptic seizures are triggered by emotional stress. Video EEG is the gold standard for diagnosing PNES. Lundukreffner syndrome leads to language regression due to ESES. Valproic acid can lower IQ in children exposed in utero. IV midazolam is crucial for treating status epilepticus without IV access. Simple febrile seizures require reassurance and follow-up. ACTH is the gold standard treatment for infantile spasms. SCN1A mutation is linked to prolonged febrile seizures. Ketogenic diet is effective for Glut1 deficiency. Long QT syndrome requires urgent EKG assessment. T itles Understanding Psychogenic Non-Epileptic Seizures Exploring Language Regression and ESES Sound Bites "The answer is SCN1A mutation." "The answer is ketogenic diet." "This is called hypercaplexia." Chapters 00:00 Introduction to Child Neurology Cases 03:04 Exploring Language Regression in Children 05:16 Status Epilepticus: Initial Treatment Strategies 06:34 Infantile Spasms and Treatment Options 07:20 Genetic Considerations in Prolonged Febrile Seizures 08:15 Understanding Glut1 Deficiency 09:02 Hypercaplexia and Its Genetic Basis 10:18 Epilepsy with Grand Mal Seizures on Awakening 11:05 Long QT Syndrome and Syncope During Exercise 11:39 Management of Juvenile Myoclonic Epilepsy in Pregnancy 12:30 Silent Ocean…

Child Neurology Board Prep

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Part 9: Pediatric Epilepsy Board Prep Q&A 11:41

منذ 10 أيام11:41

11:41

S ummary This episode of Child Neurology Board Review delves into various pediatric neurological disorders, focusing on Angelman syndrome, benign epilepsy with centrotemporal spikes, infantile spasms, temporal lobe epilepsy, and Dravet syndrome. Each condition is explored through case studies, highlighting symptoms, diagnosis, treatment options, and future directions in research and therapy. T akeaways Angelman syndrome is caused by the loss of function of the UB3A gene. Patients with Angelman syndrome exhibit developmental delays and seizures. Benign epilepsy with centrotemporal spikes is common in children and often resolves by age 18. Hypsarrhythmia is a key EEG finding in infantile spasms. Temporal lobe epilepsy can result from childhood febrile seizures. Dravet syndrome is a severe genetic epilepsy disorder triggered by fever. Avoid sodium channel blockers in Dravet syndrome as they worsen seizures. Gene therapy is a promising future direction for genetic epilepsy disorders. Early intervention and therapy are crucial for developmental outcomes. Regular follow-up is essential for managing pediatric epilepsy. Sound Bites "This is Angelman syndrome." "The diagnosis is Angelman syndrome." "This is Dravet syndrome." Chapters 00:00 Understanding Angelman Syndrome 02:50 Benign Epilepsy with Centrotemporal Spikes 05:23 West Syndrome: A Severe Infantile Epilepsy 08:07 Temporal Lobe Epilepsy and Its Implications 10:15 Dravet Syndrome: A Genetic Epilepsy Disorder 11:27 Silent Ocean…

Child Neurology Board Prep

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Part 8: Pediatric Epilepsy Board Prep Q&A 14:17

منذ 15 يومًا14:17

14:17

S ummary This episode delves into various neurological conditions in children, focusing on their diagnosis, symptoms, and management strategies. It covers congenital heart disease, DiGeorge syndrome, alternating hemiplegia of childhood, benign paroxysmal vertigo, pyridoxine-dependent epilepsy, Dravet syndrome, tonic seizures, and Lennox-Gastaut syndrome, providing insights into their clinical presentations and treatment options. T akeaways DiGeorge syndrome is characterized by low calcium and seizures. Alternating hemiplegia of childhood is caused by ATP1A3 gene mutation. Benign paroxysmal vertigo is a migraine-related disorder in children. Pyridoxine-dependent epilepsy requires IV pyridoxine for management. Dravet syndrome is linked to SCN1A gene mutations. Tonic seizures involve muscle stiffening without loss of consciousness. Lennox-Gastaut syndrome features multiple seizure types and cognitive impairment. Gene therapy is a promising future direction for rare genetic conditions. Early diagnosis and management are crucial for better outcomes. Physical and speech therapy are important for developmental support. Sound Bites "This is Dravet syndrome." "This is tonic seizure." "Gene therapy trials are ongoing." Chapters 00:00 Introduction to Child Neurology Cases 02:35 Dijon's Syndrome: Diagnosis and Treatment 04:03 Alternating Hemiplegia of Childhood: Symptoms and Management 05:48 Benign Paroxysmal Vertigo in Young Children 06:33 Pyridoxine-Dependent Epilepsy: A Rare Condition 08:00 Dravet Syndrome: Genetic Epilepsy Insights 10:00 Understanding Tonic Seizures 11:40 Lennox-Gastaut Syndrome: Complex Epilepsy Management 14:04 Silent Ocean…

Child Neurology Board Prep

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Part 7: Pediatric Epilepsy Board Prep Q&A 7:25

منذ 20 يومًا7:25

7:25

S ummary In this episode of Child Neurology Board Review, various childhood seizure disorders and their treatments are discussed. The conversation covers specific cases, diagnostic approaches, and the importance of genetic testing in identifying epilepsy syndromes. The host emphasizes the need for accurate diagnosis and appropriate treatment options for different types of seizures and related conditions in children. T akeaways Sodium valproate is the best treatment for Do syndrome. Genetic testing is crucial for diagnosing epilepsy channelopathies. Benign familial neonatal convulsion is linked to potassium channel problems. Night terrors in children are common and usually resolve by age 10. Alternating hemiplegia of childhood causes recurrent temporary weakness. Juvenile Myoclonic Epilepsy is characterized by morning myoclonic jerks. Nocturnal frontal lobe epilepsy involves intense movements during sleep. Paniopto Pless syndrome is associated with autonomic symptoms and seizures. MPSI is often caused by KCNT1 mutations. Understanding the specific type of seizure is key to treatment. Sound Bites "The only option is sodium valproate." "Night terrors go away by age 10." "This is Paniopto Pless syndrome." Chapters 00:00 Understanding Childhood Seizures and Treatments 02:23 Genetic Factors in Epilepsy 04:19 Sleep Disorders in Children 06:21 Identifying Specific Epilepsy Syndromes 07:12 Silent Ocean…

Child Neurology Board Prep

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Part 6: Pediatric Epilepsy Board Prep Q&A 10:51

منذ 22 يومًا10:51

10:51

S ummary This episode delves into various aspects of pediatric neurology, focusing on seizure management in children. It covers topics such as febrile seizures, differentiating between movement disorders and epilepsy, managing seizures in newborns, addressing medication side effects, and exploring genetic factors associated with epilepsy syndromes. The discussion emphasizes the importance of education for parents, the role of EEG in diagnosis, and the complexities of treating mixed seizure types. T akeaways Febrile seizures are common and usually do not require maintenance medications. EEG is crucial for differentiating seizures from other movement disorders. Low CSF glucose can indicate glucose transport deficiency in newborns. Topiramate can lead to serious side effects like acute angle glaucoma. Photosensitive epilepsy can be triggered by flickering lights. Diagnosis of epilepsy often relies on clinical presentation and EEG findings. Genetic mutations can be linked to specific epilepsy syndromes. Valproate is effective for a broad range of seizure types. Management of mixed seizure types requires careful medication adjustments. Education and reassurance for families are key in managing pediatric epilepsy. T itles Navigating Pediatric Seizures: A Comprehensive Guide Febrile Seizures and Beyond: Understanding Childhood Epilepsy Sound Bites "Educate the parents on seizure safety." "Diagnosis is clinical plus EEG." "This is Lend-Duk-Lefner syndrome." Chapters 00:00 Understanding Febrile Seizures and Management 02:18 Differentiating Seizures from Movement Disorders 05:04 Addressing Seizures in Adolescents and Young Adults 06:59 Genetic Factors in Epilepsy 09:15 Managing Childhood Absence Epilepsy 10:36 Silent Ocean…

Child Neurology Board Prep

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Part 5: Pediatric Epilepsy Board Prep Q&A 5:47

منذ 22 يومًا5:47

5:47

Summary This episode delves into various EEG patterns and their implications in pediatric neurology, focusing on conditions such as neonatal EEG patterns, seizures in children, and specific syndromes like Tuberous Sclerosis and Struge-Weber Syndrome. The discussion highlights the importance of understanding these patterns for accurate diagnosis and treatment. Takeaways Truss-A-alternant pattern is normal in newborns during quiet sleep. Wicket waves are harmless and a normal EEG variant. Gelastic seizures are linked to hypothalamic haematoma. Benign epilepsy with centrotemporal spikes is common in children. Infantile spasms can indicate Tuberous Sclerosis. Struge-Weber syndrome is characterized by facial capillary malformations. Lambda waves are normal during visual tasks like reading. EEG patterns can help differentiate between seizure types. MRI is crucial for diagnosing structural brain issues. Treatment options vary based on the underlying condition. Titles Decoding Neonatal EEG Patterns Seizures in Pediatric Patients Sound Bites "Wicket waves are a normal variant." "EEG shows hypserythemia in infantile spasms." "Lambda waves are a normal variant during reading." Chapters 00:00 Understanding Neonatal EEG Patterns 02:21 Identifying Seizure Types in Children 04:56 Exploring Specific Syndromes and Their Diagnosis 05:36 Silent Ocean…

Child Neurology Board Prep

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Part 4: Pediatric Epilepsy Board Prep Q&A 8:17

منذ 23 يومًا8:17

8:17

S ummary In this episode, we explore various neurological conditions, focusing on different types of epilepsy, their diagnoses, and treatment options. The conversation covers Juvenile Myoclonic Epilepsy, Lando-Kleffner Syndrome, Childhood Absence Epilepsy, and Infantile Spasms, along with the implications of anti-seizure medications during breastfeeding. Additionally, we discuss the importance of identifying EEG artifacts in clinical practice. T akeaways The diagnosis of JME is characterized by morning clumsiness and myoclonic jerks. Lando-Kleffner syndrome involves language regression and continuous spike waves on EEG. Ethosuximide is the first-line treatment for childhood absence epilepsy. Breastfeeding is generally safe for mothers on certain anti-seizure medications. Benign epilepsy with centrotemporal spikes is common in children and often resolves with age. Infantile spasms are associated with hypsarrhythmia on EEG and require prompt treatment. Identifying EEG artifacts is crucial for accurate diagnosis. Seizure management may involve adjusting medications based on patient response. Monitoring language development is important in children with epilepsy. Understanding the pathophysiology of seizures aids in effective treatment planning. T itles Decoding Neurological Episodes in Children Epilepsy Insights: JME and Beyond Sound Bites "The correct answer is JME." "It's usually safe with them." "It's called electrode pop artifact." Chapters 00:00 Introduction to Neurological Disorders in Adolescents 04:54 Exploring Absence Seizures in Children 07:43 Benign Epilepsy and Centrotemporal Spikes 08:04 Silent Ocean…

Child Neurology Board Prep

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Part 3: Pediatric Epilepsy Board Prep Q&A 12:29

منذ 25 يومًا12:29

12:29

S ummary This conversation provides an in-depth review of various types of epilepsy and seizures in children, including childhood absence epilepsy, Lennox-Gastaut syndrome, and infantile spasms. The discussion covers diagnostic criteria, EEG findings, and treatment options for each condition, emphasizing the importance of accurate diagnosis and tailored management strategies. T akeaways Childhood absence epilepsy is characterized by staring spells and EEG findings of 3 Hz spike and wave. Holoprosencephaly can lead to seizures and is associated with maternal diabetes. Lennox-Gastaut syndrome presents with multiple seizure types and severe developmental delays. Management of childhood absence epilepsy often involves ethosuximide. Benign epilepsy with centrotemporal spikes typically presents with nocturnal seizures. Juvenile myoclonic epilepsy is characterized by myoclonic jerks and requires specific treatment. Juvenile absence epilepsy can persist into adulthood and is diagnosed with specific EEG patterns. Infantile spasms are associated with chaotic brain activity and require prompt treatment. ACTH is a first-line treatment for infantile spasms unless tuberous sclerosis is present. Monitoring seizure control and developmental progress is crucial in pediatric epilepsy management. T itles Understanding Childhood Epilepsy: A Comprehensive Review Navigating Seizures in Children: Key Insights Sound Bites "This is absence epilepsy." "Typical of infantile spasm." "Ethosuximide to stop absence seizure." Chapters 00:00 Understanding Childhood Absence Epilepsy 05:46 Lennox-Gastaut Syndrome: A Complex Case 11:10 Infantile Spasms: Diagnosis and Treatment 12:15 Silent Ocean…

Child Neurology Board Prep

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Part 2: Pediatric Epilepsy Board Prep Q&A 9:04

منذ 25 يومًا9:04

9:04

S ummary This episode delves into various aspects of childhood epilepsy, focusing on specific syndromes such as West syndrome, Otahara syndrome, childhood absence seizures, and juvenile myoclonic epilepsy. The discussion includes diagnostic criteria, EEG findings, and management strategies for each condition, providing a comprehensive overview for practitioners in the field of child neurology. T akeaways West syndrome is characterized by hypsarrhythmia and infantile spasms. Temporal lobe epilepsy may require surgical intervention for drug-resistant cases. Otahara syndrome presents with burst suppression on EEG. Childhood absence seizures are identified by 3 hertz spikes on EEG. Ethosuximide is the first-line treatment for absence seizures. Juvenile myoclonic epilepsy is marked by generalized brain activity and myoclonic jerks. Seizure management should include monitoring and adjusting medications as needed. EEG findings are crucial for diagnosing different types of epilepsy. Behavioral development can be affected by various seizure types. Early intervention is key in managing childhood epilepsy effectively. T itles Navigating Childhood Epilepsy: Key Insights Understanding West Syndrome in Pediatric Patients Sound Bites "The most likely diagnosis is West syndrome." "Hypsarrhythmia is typical of West syndrome." "Monitor seizure control and increase sleep." Chapters 00:00 Understanding Infantile Spasms and West Syndrome 00:23 New Chapter 02:36 Exploring Otahara Syndrome in Newborns 05:12 Identifying Hypothalamic Hamartoma and Its Implications 06:18 Recognizing Childhood Absence Seizures 06:18 Understanding Focal Epilepsy Management 08:50 Silent Ocean…

Child Neurology Board Prep

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Part 1: Pediatric Epilepsy Board Prep Q&A 11:56

منذ 26 يومًا11:56

11:56

S ummary This episode of Child Neurology Board Review focuses on pediatric epilepsy, discussing various types of seizures, their diagnoses, and treatment options. The conversation covers cases of benign epilepsy with centrotemporal spikes, infantile spasms, juvenile myoclonic epilepsy, Lennox-Gastaut syndrome, and childhood occipital epilepsy, providing insights into their pathophysiology and management strategies. T akeaways Benign epilepsy with centrotemporal spikes is likely to outgrow. Absence seizures are characterized by short staring spells. Infantile spasms are linked to tuberous sclerosis complex. Juvenile myoclonic epilepsy presents with myoclonic jerks. Lennox-Gastaut syndrome involves multiple seizure types and developmental delay. Childhood occipital epilepsy can cause autonomic symptoms like vomiting. EEG is crucial for diagnosing different types of epilepsy. Treatment options vary based on the type of epilepsy. Regular follow-ups are essential for managing pediatric epilepsy. Understanding the prognosis helps in counseling families. T itles Understanding Pediatric Epilepsy: A Comprehensive Review Exploring the Spectrum of Pediatric Epilepsy Sound Bites "He has a form of epilepsy that he likely to outgrow." "This is absence seizure, childhood absence epilepsy." "This is classic JME, juvenile myoclonic epilepsy." Chapters 00:00 Introduction to Pediatric Epilepsy 02:10 Understanding Benign Epilepsy with Centrotemporal Spikes 04:13 Exploring Infantile Spasms and Tuberous Sclerosis 05:52 Juvenile Myoclonic Epilepsy: Diagnosis and Treatment 08:15 Lennox-Gastaut Syndrome: A Complex Case 09:53 Occipital Epilepsy: Symptoms and Management 11:39 Silent Ocean…

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Navigating Career Pivots and Grit with Milo’s Avni Patel Thompson 26:18

Child Neurology Board Prep

Child Neurology Board Prep

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Part 10: Pediatric Epilepsy Board Prep Q&A 12:42

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Part 9: Pediatric Epilepsy Board Prep Q&A 11:41

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Part 8: Pediatric Epilepsy Board Prep Q&A 14:17

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Part 7: Pediatric Epilepsy Board Prep Q&A 7:25

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Part 6: Pediatric Epilepsy Board Prep Q&A 10:51

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Part 5: Pediatric Epilepsy Board Prep Q&A 5:47

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Part 4: Pediatric Epilepsy Board Prep Q&A 8:17

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Part 3: Pediatric Epilepsy Board Prep Q&A 12:29

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Part 2: Pediatric Epilepsy Board Prep Q&A 9:04

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Part 1: Pediatric Epilepsy Board Prep Q&A 11:56

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The Let Them Theory: A Life-Changing Tool That Millions of People Can't Stop Talking About

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Child Neurology Board Prep

Child Neurology Board Prep

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The Let Them Theory: A Life-Changing Tool That Millions of People Can't Stop Talking About

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