Assuming main is required, the following 98 results were found.
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Confusinghttps://cnke.org/article-flags/336
to enhance its readability and comprehension. Clear and well-structured content is essential to ensure CNKE.org remains a reliable and accessible resource for the child neurology community. Suggestions for Improvement: Simplify Complex Sentences: Break...
- Type: Article
- Author: Editor CNKE
- Category: Article Flags
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Thomas testhttps://cnke.org/articles/181
mechanisms in gait abnormalities. Procedure: Position the patient supine on an examination table. Ensure the pelvis remains neutral (no anterior/posterior tilt). Ask the patient to hold one knee (unaffected/contralateral side) close to their chest to...
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- Author: Editor
- Category: Home
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Malignant Hyperthermiahttps://cnke.org/articles/238
individuals. Prognosis: With prompt diagnosis and treatment, the outcomes of MH have improved significantly. However, it remains a critical cause of anesthesia-related morbidity and mortality.
- Type: Article
- Author: Editor CNKE
- Category: Articles
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Psychometric measureshttps://cnke.org/articles/197
psychometric measures used in the developmental and neuropsychaological assessment of children based on the domains they assess. General Cognitive Ability Wechsler Intelligence Scale for Children (WISC-V) Stanford-Binet Intelligence Scales (SB5) Kaufman...
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- Author: Editor CNKE
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Measures for Hypertonia, Ataxia, and Ticshttps://cnke.org/articles/198
body parts. Ataxia-Specific Tools Scale for the Assessment and Rating of Ataxia (SARA): Rates severity of ataxia across domains like gait, stance, and coordination. International Cooperative Ataxia Rating Scale (ICARS): Assesses postural control,...
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- Author: Editor CNKE
- Category: Articles
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Investigations of the baby with abnormal neurologyhttps://cnke.org/articles/317
for the typical SMN gene deletion confirms the clinical diagnosis. Findings on EMC and muscle biopsy are nonspecific and mainly allow the exclusion of other disorders pending the results of the molecular genetic studies. {tabulizer:include...
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- Author: Editor
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Investigating Lysosomal disordershttps://cnke.org/articles/163
used in lysosomal storage diseases to denote the situation in which individuals show greatly reduced enzyme activity but remain clinically healthy. Pseudodeficiencies have been reported for several lysosomal hydrolases. Pseudodeficiency is particularly...
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- Author: ICNA
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Benign Familial Infantile Seizureshttps://cnke.org/articles/275
Epidemiology Global Reports: BFIE cases have been reported worldwide. Prevalence and Incidence: Remain unknown. Clinical Description Age of Onset: Seizures usually occur between 3 to 8 months of life. Seizure Characteristics: Clusters of 8-10 episodes...
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- Author: Editor
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Wilder Graves Penfieldhttps://cnke.org/articles/296
epilepsy. This procedure involves removing the part of the brain where seizures originate. During the surgery, patients remain conscious under local anesthesia, allowing Penfield to stimulate different parts of the brain with electrical probes. This...
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- Author: Editor
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Zika Virus Infectionhttps://cnke.org/articles/353
been confirmed (Besnard et al., 2014). Humans are the primary host for Zika virus. Approximately 80% of infected persons remain asymptomatic (Hayes, 2009; Duffy et al., 2009). The disease when symptomatic is generally mild and characterized by acute...
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- Author: Editor
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Ion channel disordershttps://cnke.org/articles/231
in children). Genetic Testing: Identifies mutations in: CACNA1S gene (~70% of cases). SCN4A gene (~12% of cases). ~20% remain genetically undefined, suggesting further heterogeneity. Differential Diagnosis: Secondary causes of hypokalemia: Primary...
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- Author: Editor CNKE
- Category: Articles
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Posterior Fossa Syndrome (PFS)https://cnke.org/articles/248
modulation, and vowel/consonant articulation. Comprehensive rehabilitation improves outcomes, though residual deficits may remain. Posterior Fossa Syndrome is a multifaceted postoperative complication with significant impacts on motor, speech,...
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- Author: Editor CNKE
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Developmental Milestones (Birth to 8 Years)https://cnke.org/articles/166
more complex sentences Engages in detailed storytelling Key Considerations Developmental milestones vary; delays in one domain may not indicate overall developmental issues. Early intervention is critical for any suspected delays, especially in...
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- Author: Editor
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Night Terrors https://cnke.org/articles/230
stages 3 and 4 non-rapid eye movement sleep. Night terrors are most common in between ages 4 until puberty. The three main stages of sleep are (1) wakefulness, (2) non-rapid eye movement (non-REM) sleep, and (3) rapid eye movement (REM) sleep. These...
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- Author: Editor
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MED12L Variant and Its Role in Human Diseasehttps://cnke.org/articles/360
II machinery, thereby facilitating the transcription of nearly all protein-coding genes. The complex is divided into four main modules: Head Module: This module interacts directly with RNA polymerase II, playing a critical role in the formation and...
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- Author: Editor
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Cerebrotendinous Xanthomatosis (CTX)https://cnke.org/articles/146
High Suspicion (9+ points): Strongly consider CTX; initiate confirmatory testing and treatment immediately. Management Main Treatment: Chenodeoxycholic Acid (CDCA) Mechanism: Restores bile acid synthesis. Lowers plasma and CSF cholestanol levels....
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- Author: Editor
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Idiopathic Intracranial Hypertensionhttps://cnke.org/articles/178
childbearing age. Prevalence: Ranges from 0.5–2 per 100,000, increasing with the global rise in obesity. Clinical Features Main Symptoms: Headache: Frequently migrainous in phenotype; may persist after ICP normalization. Visual Alterations:...
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- Author: Editor
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Inherited Cerebellar Ataxias (ICAs)https://cnke.org/articles/184
Square wave jerks, hypometric slow saccades, vertical supranuclear saccades palsy Cerebellar ataxias according to main clinical features Cerebellar Cognitive Affective Syndrome (CCAS) Also known as Schmahmann’s syndrome Includes executive deficits,...
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- Author: Editor CNKE
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