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Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
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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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The clinical conditions affecting the skeletal muscle tissue are broadly categorized as musculoskeletal and neuromuscular disorders.
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Thoracic, aortic arch and abdominal aneurysms are significant vascular conditions that can present with various clinical manifestations and lead to serious complications. Understanding these manifestations and the appropriate diagnostic studies is essential for effective management and treatment.Thoracic Aortic AneurysmsThoracic aortic aneurysms often remain asymptomatic until they reach a size that impinges on adjacent structures. They typically cause deep, diffuse chest pain that radiates to...
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Pleiotropy01:33

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Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
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Acute Coronary Syndrome I: Introduction01:30

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Acute Coronary Syndrome (ACS) encompasses a spectrum of heart conditions caused by sudden obstruction of coronary arteries, typically resulting from the rupture of an atherosclerotic plaque and subsequent thrombus (blood clot) formation. This obstruction can lead to partial or complete blockage of blood flow, causing varying degrees of myocardial ischemia or infarction.ACS includes the following clinical entities:Unstable Angina (UA)Non-ST-Elevation Myocardial Infarction (NSTEMI)ST-Elevation...
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A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
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Sweyr-James-MacLeod syndrome: a case report.

Doaa Abo Hamza1, Sawssan Ali1, Maha Alshahen2

  • 1Pediatric Hospital, Damascus University, Damascus, Syria.

International Journal of Surgery Case Reports
|December 3, 2025
PubMed
Summary
This summary is machine-generated.

Swyer-James-MacLeod syndrome (SJMS) is a rare lung condition in children. Early diagnosis and surgical intervention like lobectomy can effectively treat localized, severe cases, preventing long-term lung damage.

Area of Science:

  • Pediatric Pulmonology
  • Thoracic Surgery

Background:

  • Swyer-James-MacLeod syndrome (SJMS) is a rare acquired pulmonary disorder affecting children.
  • Characterized by unilateral lung hyperlucency, bronchiectasis, and recurrent respiratory symptoms, timely diagnosis is crucial.
Keywords:
BronchiectasisCase reportLobectomyPediatricSwyer-James-MacLeod syndromeUnilateral hyperlucency

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