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Related Concept Videos

Pleiotropy01:33

Pleiotropy

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,...
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

Smooth endoplasmic reticulum or smooth ER is a sub-organelle with specialized functions in animal cells and plant cells. It is often associated with the tubule morphology of the endoplasmic reticulum.
The ER provides optimal conditions for synthesizing steroid hormones and lipids, such as phospholipids and triglycerides. Traditionally, lipid metabolism was considered to be a smooth ER function. However, there is no direct evidence to prove that rough ER is completely excluded from lipid...
Esophageal Achalasia01:27

Esophageal Achalasia

Esophageal achalasia is a chronic neurogenic disorder characterized by impaired relaxation of the lower esophageal sphincter (LES) and absent or ineffective peristalsis in the distal esophagus. This leads to a functional obstruction without a physical blockage, despite significant disruption of esophageal motility.EtiologyAchalasia is caused by degeneration of the myenteric (Auerbach's) plexus, specifically the loss of inhibitory ganglion cells that produce vasoactive intestinal peptide (VIP)...
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Notch Signaling Pathway

The Notch signaling pathway is a major intracellular signaling pathway that is highly conserved over a broad spectrum of metazoan species. It stands unique from other intracellular signaling mechanisms in animals because notch protein itself acts as the receptor as well as the primary signaling molecule.
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Cushing Syndrome II: Pathophysiology

Cortisol production is normally governed by the hypothalamic–pituitary–adrenal (HPA) axis, which maintains hormonal balance through tightly regulated feedback mechanisms. Disruption of this regulatory system is central to the development of Cushing syndrome, whether the excess cortisol originates from external medications or internal pathology. Persistent cortisol elevation alters metabolism, immune function, and endocrine signaling, producing the characteristic clinical features of the...
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Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:

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The effects of iloprost on ischemia-reperfusion injury in skeletal muscles in a rodent model.

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Related Experiment Video

Updated: Jul 14, 2026

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome
09:39

Generation of Induced Pluripotent Stem Cells from Turner Syndrome (45XO) Fetal Cells for Downstream Modelling of Neurological Deficits Associated with the Syndrome

Published on: December 4, 2021

Paget-Schroetter syndrome.

Gursel L Oktar1, Emin G Ergul

  • 1Division of Cardiovascular Surgery, Ankara Oncology Training and Research Hospital, Ankara, Turkey. loktar@isnet.net.tr

Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi
|June 6, 2007
PubMed
Summary

Paget-Schroetter syndrome, or effort thrombosis, is a rare deep vein thrombosis caused by strenuous arm activity. Early diagnosis and appropriate management are crucial to prevent long-term disability from post-thrombotic syndrome.

Area of Science:

  • Vascular Surgery
  • Thrombosis Research
  • Sports Medicine

Background:

  • Paget-Schroetter syndrome (PSS), also known as effort thrombosis, is an uncommon deep vein thrombosis (DVT) affecting the axillary-subclavian veins.
  • It typically results from repetitive strenuous upper extremity activity, leading to venous compression and thrombus formation.
  • Untreated PSS can progress to debilitating post-thrombotic syndrome (PTS).

Observation:

  • This report details a case of PSS in a young male weightlifter, a demographic susceptible to exertional venous injuries.
  • The patient's presentation highlights the clinical manifestations of PSS in an athletic individual.
  • The case underscores the importance of considering PSS in young, active individuals presenting with upper extremity swelling and pain.

Findings:

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  • The optimal management for PSS remains debated due to limited evidence from small studies.
  • Treatment strategies discussed include anticoagulation, thrombolysis, and surgical decompression, with varying success rates.
  • This case illustrates the diagnostic and therapeutic challenges associated with PSS.

Implications:

  • Prompt diagnosis and tailored treatment are essential to mitigate the risk of PTS and long-term arm dysfunction.
  • Further research with larger cohorts is needed to establish evidence-based guidelines for PSS management.
  • This case contributes to the understanding of PSS in athletes and informs clinical decision-making.