Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Klippel-Trenaunay syndrome.

S Sethi1, B S Shubha

  • 1Department of Pathology, Lady Hardinge Medical College, and Smt. Sucheta Kriplani Hospital, New Delhi-110001, India. drsethi@hotmail.com

Indian Journal of Pediatrics
|September 21, 2001
PubMed
Summary

Klippel Trenaunay syndrome is a rare congenital disorder with vascular anomalies. Early clinical recognition and prenatal diagnosis are crucial for managing this condition.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Trans-Tasman Comparison of Microbial Trends and Antibiotic Resistance Patterns in Severe Odontogenic Infection: A 5-Year Retrospective Analysis of South Australia, Australia and Auckland, New Zealand.

Australian dental journal·2026
Same author

Perspectives of Dental Stakeholders on the Clinical Use of Silver Diamine Fluoride in Australia for Caries.

JDR clinical and translational research·2025
Same author

Discrimination and Oral Health Impact: Moderating Role of Sex and Sexuality.

Journal of dental research·2025
Same author

Pediatric non-traumatic dental presentations to the emergency department: a ten year retrospective study in an Australian tertiary hospital.

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2024
Same author

Reply to the Letter to the Editor regarding 'PFS, OS or toxicity: what is the most important factor in the treatment of EGFR-mutated lung cancer?' by T. Nishimura and H. Fujimoto.

Annals of oncology : official journal of the European Society for Medical Oncology·2024
Same author

"It's Everybody's and It's Nobody's Responsibility": Stakeholder Perspectives on Aboriginal and Torres Strait Islander Health Equity at the Nexus of Chronic Kidney Disease and Oral Health.

JDR clinical and translational research·2024

Area of Science:

  • Medical Genetics
  • Vascular Biology
  • Congenital Disorders

Background:

  • Klippel Trenaunay syndrome (KTS) is a rare congenital disorder.
  • It is characterized by a triad of vascular malformations, soft tissue hypertrophy, and bone abnormalities.
  • KTS can lead to life-threatening complications, necessitating careful management.

Observation:

  • This report presents a clinical case of Klippel Trenaunay syndrome.
  • The case highlights the importance of recognizing the syndrome's diverse manifestations.
  • Emphasis is placed on the diagnostic challenges and clinical significance.

Findings:

  • The presented case underscores the variability in KTS presentation.
  • Clinical recognition is paramount for timely intervention.
  • Prenatal diagnosis and genetic counseling are vital components of care.

Implications:

  • Improved understanding of KTS clinical significance can aid early diagnosis.
  • Enhanced prenatal counseling can support affected families.
  • Further research into KTS pathogenesis may reveal novel therapeutic targets.

Related Experiment Videos