Assuming main is required, the following 98 results were found.
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The Cherry Red Spothttps://cnke.org/articles/170
cells. Retained red appearance of the fovea because it lacks ganglion cells, allowing the choroidal vasculature to remain visible. Time-dependent changes: Cherry-red spot may fade as surrounding ganglion cells atrophy. Ethnic variability: Retinal...
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- Author: Editor
- Category: Home
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Augmentative and Alternative Communication (AAC)https://cnke.org/articles/250
again. AAC is a vital tool for supporting children with severe speech impairments, enabling them to communicate effectively, maintain social interactions, and enhance their overall quality of life. Early assessment, personalized intervention, and...
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- Author: Editor CNKE
- Category: Articles
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Hopkins syndromehttps://cnke.org/articles/hopkins-syndrome
Hypoxic Contribution: Hypoxia during severe asthma episodes may exacerbate neuronal injury, although the exact mechanism remains speculative. Clinical Manifestations Core Features Acute Flaccid Paralysis (AFP): Typically asymmetric, involving one or...
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- Author: Editor
- Category: Home
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Terms and Conditionshttps://cnke.org/about/172
or collective economic actions to prevent antitrust liability. Any discussions of reimbursement policies should remain within legal bounds and must not lead to anti-competitive practices. No Medical Advice The Licensed Content is intended solely for...
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- Author: Editor CNKE
- Category: About
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Guillaume Duchenne (1806–1875)https://cnke.org/historical-vignettes/175
His meticulous clinical descriptions of pseudohypertrophy of the calves, proximal muscle weakness, and disease progression remain central to understanding DMD. Duchenne-Aran Spinal Muscular Atrophy: A form of progressive muscular atrophy distinguished...
- Type: Article
- Author: Biju Hameed
- Category: Historical Vignettes
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Clean Uphttps://cnke.org/article-flags/334
defined, unverified, or overly indiscriminate, potentially affecting the clarity and reliability of the information. To maintain CNKE.org’s quality standards, these elements require review and refinement. Specific Issues to Address: Poorly Defined Lists...
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- Author: Editor CNKE
- Category: Article Flags
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Schwartz–Jampel Syndromehttps://cnke.org/articles/237
which encodes perlecan: A heparan sulfate proteoglycan found in basement membranes and cartilage. Perlecan is critical for maintaining the structural integrity of cartilage and other connective tissues. Diagnosis: Clinical Diagnosis: Based on...
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- Author: Editor CNKE
- Category: Articles
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Henri Gastaut [1915 - 1955]https://cnke.org/articles/362
later donating his collection to a museum. Retired from medicine and science, focusing on politics in his later years. Maintained connections with the village of Les Lecques, where he lived for over 40 years. Survived by his three children, all residing...
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- Author: Editor
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with repositioning and physiotherapy. Age at initiation: Optimal between 4-6 months when skull growth is rapid and sutures remain open. Ineffectiveness beyond 12-18 months due to reduced cranial plasticity. Process Custom helmet is made after a detailed...
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- Author: Editor
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Facioscapulohumeral muscular dystrophy https://cnke.org/articles/226
myopathies, and certain limb-girdle muscular dystrophies (e.g., LGMD2A). Management: Supportive Care: Physiotherapy for maintaining strength and mobility. Analgesics and exercise programs for myalgia. Orthopedic support for joint and postural issues....
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- Author: Editor CNKE
- Category: Articles
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Nesprinopathieshttps://cnke.org/articles/318
This complex contributes to nuclear positioning and cellular vitality, establishing nuclear-cytoskeletal connections and maintaining cellular architecture (Rajgor et al., 2013). Nesprin Genes and Isoforms Four nesprin genes: SYNE1, SYNE2, SYNE3, and...
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- Author: Editor
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USP7 related disordershttps://cnke.org/articles/147
difficulties often diagnosed as intellectual disability (ID). Educational needs range from special education programs to mainstream schooling with an Educational Health Care Plan (EHCP). Behavioral Challenges: Autistic traits: Hand flapping, repetitive...
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- Author: Editor
- Category: Home
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Neurofibromatosishttps://cnke.org/articles/283
in children with NF1. Study Findings: 81% of children with NF1 have moderate to severe impairment in one or more cognitive domains. IQ Scores: 5 to 10 points lower compared to the general population or unaffected sibling controls. Incidence of...
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- Author: Editor
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Copy Editing Issueshttps://cnke.org/article-flags/338
standards for grammar, style, cohesion, tone, and spelling. Attention to these elements will improve readability and maintain the professional tone expected of a trusted child neurology resource. Areas to Focus On: Grammar and Syntax: Check for and...
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- Author: Editor CNKE
- Category: Article Flags
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Myotonic Dystrophyhttps://cnke.org/articles/229
dystrophy often present with: Static Cognitive Issues: Cognitive impairments may manifest during childhood, typically remaining stable over time. Muscle Weakness: Weakness is generally mild and proximally predominant, often not significantly impacting...
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- Author: Editor CNKE
- Category: Articles
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New Article Submission Policy and Procedurehttps://cnke.org/about/173
of their work. Peer Review CNKE.ORG functions as a collaborative Wiki. Articles are subject to regular editorial review to maintain accuracy but are not formally peer-reviewed. By adhering to these policies, contributors help ensure that CNKE.ORG...
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- Author: Editor
- Category: About
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Guidance on article flagginghttps://cnke.org/about/guidance-on-article-flagging
At CNKE.Org, we encourage thoughtful and constructive contributions to maintain the highest standards of accuracy and relevance in our content. While flagging articles for issues like factual inaccuracies or unclear content is an essential part of the...
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- Author: Editor CNKE
- Category: About
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Alexander Diseasehttps://cnke.org/articles/253
cases). Adult Form: 33% (96/293 cases). Asymptomatic Individuals: 3% (10/293 cases). Clinical status of these individuals remains unknown. Historical Classification Neonatal Form: Sometimes considered a subset of the infantile form. Severe and rapidly...
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- Author: Editor CNKE
- Category: Articles
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Speech and Language developmental disordershttps://cnke.org/articles/243
in auditory processing, phonology, lexical access, or semantics. Specific Language Impairment (SLI) Debated Causes: Domain-Specific Deficit: Affects grammar or linguistic structures. Processing Deficit: Issues with auditory temporal processing Cognitive...
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- Author: Editor CNKE
- Category: Articles
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Benign familial neonatal epilepsyhttps://cnke.org/articles/266
epileptic syndrome characterised by frequent brief seizures within the first days of life. Clinical features Seizures mainly occur in full-term normal neonates following a normal pregnancy and delivery and without precipitating factors. Seizures are...
- Type: Article
- Author: Editor
- Category: Home