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Monday, 06 January 2025

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Editor

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Assuming main is required, the following 97 results were found.

  1. Self Injurious Behaviour (SIB) https://cnke.org/articles/32

    of understanding the purpose that behavior serves for the person.After identifying the antecedents and consequences that maintain SIB through an FBA, it is possible to hypothesize about the function(s) of the behavior(s). Research indicates that...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  2. Dravet syndromehttps://cnke.org/articles/180

    children exhibit difficult behaviour with hyperactivity and severe learning difficulties Developmental delay affects all domains with the motor, linguistic, and visual abilities being affected the most Behavior is often marked by hyperactivity,...

    • Type: Article
    • Author: Editor
    • Category: Home

  3. Dravet syndromehttps://cnke.org/articles/265

    children exhibit difficult behaviour with hyperactivity and severe learning difficulties Developmental delay affects all domains with the motor, linguistic, and visual abilities being affected the most Behavior is often marked by hyperactivity,...

    • Type: Article
    • Author: Editor
    • Category: Home

  4. How to edit this Knowledge Basehttps://cnke.org/about/182

    only be made possible through collaborative content authoring. There are several ways you can get involved in creating and maintaining this child neurology knowledge environment. A great way to start is by contributing articles to the Child Neurology...

    • Type: Article
    • Author: Editor
    • Category: About

  5. Lennox-Gastaut Syndrome (LGS)https://cnke.org/articles/50

    problems noted in most patients (75 to 99%) within five years of onset. A minority (10–20%) of affected children remain within the accepted limits of normal intellectual function but often face difficulties in everyday life due to a slowing of mental...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  6. Cerebellar ataxias according to main clinical featureshttps://cnke.org/articles/183

    Type 1 (AOA1), often accompanied by mild intellectual deficiency. Spastic Ataxia and Related Disorders SCAR12/WWOX (WW Domain-Containing Oxidoreductase Mutation) Found in SCAR12, with intellectual disability, seizures, and ataxia. SCAR22/VWA3B (Von...

    • Type: Article
    • Author: Editor
    • Category: Home

  7. The Normal EEG in Childrenhttps://cnke.org/articles/25

    as the background can be attenuated by eye opening as early as age 3 months. Gentle passive closure of the eyes can be maintained for a few seconds. A low frequency filter (LFF) of 1 Hz might be helpful to decrease the quantity of movement artifact at...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  8. Duchenne Muscular Dystrophyhttps://cnke.org/articles/225

    Clinical Features: Independent ambulation typically persists beyond age 16. Variable onset of weakness; some individuals remain ambulant throughout life. Cardiac Manifestations: Higher incidence of symptomatic cardiomyopathy compared to DMD. Key...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  9. Valproatehttps://cnke.org/articles/287

    Dosage and Titration Adults: Initial dose: 200 mg/day in two divided doses for 3 days. Increment: 200 mg/day every 3 days. Maintenance: 1000–1500 mg/day (max 3000 mg/day). Children: Initial dose: 10 mg/kg/day. Increment: 10 mg/kg/day every 3 days....

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    • Author: Editor
    • Category: Home

  10. Circadian Rhythm Sleep-Wake Disorders (CRSWD)https://cnke.org/articles/164

    that orchestrate physiological, behavioral, and molecular processes across the human body. These rhythms are foundational to maintaining homeostasis and are synchronized with environmental cues, such as light and temperature, by a central pacemaker in...

    • Type: Article
    • Author: Editor
    • Category: Home

  11. Charcot–Marie–Tooth disease (CMT)https://cnke.org/articles/214

    loss. Areflexia (loss of reflexes). Genetic Basis Causative Mechanisms: Disorders of genes affecting: Myelin compaction and maintenance. Cytoskeletal formation. Axonal transport. Mitochondrial metabolism. Inheritance Patterns: Autosomal dominant....

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  12. Familial (Autosomal Dominant) Focal Epilepsieshttps://cnke.org/articles/357

    from normal phenomena in cases with mild and infrequent seizures of predominantly déjà vu can be challenging. Main differentiating features from hippocampal epilepsy: Onset in teens or early adult life No febrile convulsions or other antecedent factors...

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    • Author: Editor
    • Category: Home

  13. Multiminicore Diseasehttps://cnke.org/articles/multiminicore-disease

    and genetically heterogeneous congenital myopathy characterized by multiple small cores in muscle fibers on biopsy. Main Forms: Rigid Spine Muscular Dystrophy Type 1 (RSMD1): Caused by recessive SEPN1 mutations. RYR1-related Multiminicore Myopathy:...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  14. Nemaline Myopathy (NM)https://cnke.org/articles/219

    Protein: Cofilin 2. Clinical Features: Only two families reported. No facial weakness or foot drop. Kelch repeat and BTB domain-containing 13 (KBTBD13) Inheritance: AD. Protein: Kelch repeat protein. Clinical Features: Childhood onset. Proximal weakness...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  15. Why a Lecture Notes Style Knowledgebase on Child Neurology?https://cnke.org/about/180

    by integrating perspectives from various regions, subspecialties, and experiences, enriching the knowledgebase while maintaining a standardized structure. Enhanced Focus on Practical Application By prioritizing concise, actionable information over...

    • Type: Article
    • Author: Editor
    • Category: About

  16. Comparitive genomic hybridization (CGH) https://cnke.org/articles/288

    children with unexplained mental retardation, autism, or congenital anomalies and in unaffected persons. These imbalances remain undetectable using routine karyotype analysis.The use of array comparative genomic hybridization is thus replacing the use...

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    • Author: Editor
    • Category: Home

  17. Infantile Spasms Syndromehttps://cnke.org/articles/269

    to: 77% of patients with unilateral brain involvement 92% with bilateral brain involvement (Raches D et al., 2012) Seizures mainly partial and tonic-clonic generalized types (Raches D et al., 2012) ISs sporadically recorded (Raches D et al., 2012)...

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    • Author: Editor
    • Category: Home

  18. Progressive myoclonus epilepsy https://cnke.org/articles/258

    progressive myoclonus and cerebellar ataxia. Proper management: Can avert dementia, minimize myoclonus and seizures, and maintain a normal lifespan (Lehesjoki 2002). Preferred anticonvulsants: Valproic acid, zonisamide, and levetiracetam. Piracetam...

    • Type: Article
    • Author: Editor
    • Category: Home

  19. Glycosylphosphatidylinositol (GPI) Anchor and Glycosphingolipid (GSL) Related Disordershttps://cnke.org/articles/476

    structures that tether proteins to the cell membrane. Functions: Facilitate protein sorting into specialized lipid domains (lipid rafts). Involved in signaling, immune response, and enzymatic activity. Critical for neural development and synaptic...

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    • Author: Editor
    • Category: Home

  20. PRRT2-Associated Disordershttps://cnke.org/articles/274

    protein 2. PRRT2 protein helps regulate signaling in the brain. Composed of a proline-rich extracellular N-terminal domain and a membrane-bound C-terminal domain. PRRT2 Protein Interactions Protein Interactions: The PRRT2 protein interacts with several...

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    • Author: Editor
    • Category: Home
Results 1 - 20 of 97