Related Experiment Video
Updated: Jul 3, 2026

06:48
Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome
Published on: March 23, 2022
[Klippel-Trenaunay-Weber syndrome].
Murat Ugurlucan1, Can Yerebakan, Ufuk Alpagut
1Abteilung für Herz- und Gefässchirurgie, Medizinische Fakultät, Istanbul Universität, Turkey. can.yerebakan@med.uni-rostock.de
Wiener Medizinische Wochenschrift (1946)
|August 5, 2008
Summary
Klippel-Trenaunay syndrome, a rare inherited disorder, can affect arteries. This case highlights arterial aneurysms and stenosis in a child with Klippel-Trenaunay-(Weber) syndrome.
Area of Science:
- Vascular Medicine
- Genetics
- Pediatric Cardiology
Background:
- Klippel-Trenaunay syndrome is a congenital disorder primarily affecting the venous system.
- Vascular anomalies in Klippel-Trenaunay syndrome typically involve venous malformations.
- Arterial pathologies are exceptionally rare in this condition.
Observation:
- A 7-year-old boy presented with Klippel-Trenaunay-(Weber) syndrome.
- The patient exhibited unusual arterial complications.
- Iliac and femoral artery aneurysms and stenosis were identified in the lower limb.
Findings:
- This report details a rare presentation of arterial stenosis and aneurysms in Klippel-Trenaunay-(Weber) syndrome.
- The arterial involvement occurred at multiple levels within the lower limb's vasculature.
- The coexistence of venous and arterial anomalies underscores the syndrome's complex vascular manifestations.
Implications:
- Highlights the potential for rare arterial complications in Klippel-Trenaunay syndrome.
- Suggests the need for comprehensive vascular assessment in affected children.
- Contributes to understanding the spectrum of vascular anomalies in genetic syndromes.
More Related Videos
Related Concept Videos
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,...
Sex Linked Disorders
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.
Sex-linked Disorders
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.
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.
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not until 1985...
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not until 1985...
Routh-Hurwitz Criterion II
In the application of the Routh-Hurwitz criterion, two specific scenarios can arise that complicate stability analysis.
The first scenario occurs when a singular zero appears in the first column of the Routh table. This situation creates a division by zero issues. To resolve this, a small positive or negative number, denoted as epsilon (∈), is substituted for the zero. The stability analysis proceeds by assuming a sign for ∈. If ∈ is positive, any sign change in the first column of the Routh...
The first scenario occurs when a singular zero appears in the first column of the Routh table. This situation creates a division by zero issues. To resolve this, a small positive or negative number, denoted as epsilon (∈), is substituted for the zero. The stability analysis proceeds by assuming a sign for ∈. If ∈ is positive, any sign change in the first column of the Routh...
[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement
The Claisen rearrangement is a [3,3] sigmatropic rearrangement of allyl vinyl ethers to unsaturated carbonyl compounds. The rearrangement is a concerted pericyclic reaction proceeding via a chair-like transition state.

