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Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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Genome-wide Association Studies-GWAS01:11

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
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Nephrotic Syndrome II : Assessment and Medical Management01:26

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IntroductionNephrotic syndrome is a kidney disorder marked by excessive protein loss in the urine, leading to various systemic complications. This condition often results from damage to the glomeruli—the kidney's filtering units—causing proteinuria, low blood protein levels, and fluid retention. Understanding the assessment, diagnosis, and management of nephrotic syndrome is essential for effective treatment and prevention of further kidney damage.AssessmentPatient History: Document...
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Incomplete Dominance01:43

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Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
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Nephrotic Syndrome I : Introduction01:24

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Nephrotic Syndrome is a chronic kidney disorder defined by clinical findings such as severe proteinuria, hypoalbuminemia, hyperlipidemia, and edema. These symptoms result from damage to the glomeruli, the kidney’s filtering units, increasing their permeability to proteins.Definition and Meaning:Proteinuria, defined as the loss of more than 3.5 grams of protein per day in adults, is a crucial feature of nephrotic syndrome. This condition is often accompanied by edema, the accumulation of...
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Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation01:21

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Clinical manifestationsPeripheral Arterial Disease (PAD) manifests through a range of symptoms, from the characteristic intermittent claudication to atypical presentations and severe complications in advanced stages. Intermittent claudication, a hallmark symptom of PAD, presents as exercise-induced muscle pain that typically resolves within minutes of rest. This pain is reproducible and stems from inadequate blood flow, leading to the accumulation of lactic acid produced during anaerobic...
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Related Experiment Video

Updated: Aug 12, 2025

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
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[Sneddon-Wilkinson disease: a case report].

Sara Kerroum1, Najoua Ammar1, Kaoutar Znati2

  • 1Centre Hospitalier Universitaire Ibn Sina, Service de Dermatologie-Vénérologie, Faculté de Médecine et de Pharmacie, Université Mohamed V, Rabat, Maroc.

The Pan African Medical Journal
|February 1, 2023
PubMed
Summary
This summary is machine-generated.

Sneddon-Wilkinson disease is a benign neutrophilic dermatosis presenting with pustular lesions. This case report details a 49-year-old patient diagnosed with this relapsing-remitting condition.

Keywords:
Subcorneal pustulosis (Sneddon-Wilkinson disease)case reportdapsone

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Area of Science:

  • Dermatology
  • Immunodermatology

Background:

  • Sneddon-Wilkinson disease is a rare neutrophilic dermatosis.
  • It is characterized by pustular lesions on the trunk and skin folds.
  • The condition has a relapsing-remitting course and may associate with other diseases.

Observation:

  • A 49-year-old patient presented with amicrobial pustulosis.
  • The patient exhibited characteristic clinical features of Sneddon-Wilkinson disease.

Findings:

  • Diagnosis of Sneddon-Wilkinson disease confirmed in the patient.
  • This highlights the importance of recognizing its distinct clinical presentation.

Implications:

  • Early diagnosis and management are crucial for patients with Sneddon-Wilkinson disease.
  • Regular follow-up is necessary due to potential associations with other conditions.
  • Dapsone remains the first-line therapy for this benign pustulosis.