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 Concept Videos

Pleiotropy01:33

Pleiotropy

40.7K
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,...
40.7K
Sex-linked Disorders01:43

Sex-linked Disorders

102.4K
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.
102.4K
Smooth Endoplasmic Reticulum01:21

Smooth Endoplasmic Reticulum

5.9K
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...
5.9K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

17
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
17
Disorders of the Female Reproductive System01:24

Disorders of the Female Reproductive System

421
The female reproductive system can be affected by several disorders, including Premenstrual Syndrome (PMS), Premenstrual Dysphoric Disorder (PMDD), endometriosis, and various forms of cancer. PMS and PMDD are cyclical conditions that cause physical and emotional distress, with symptoms that include edema, mood swings, and food cravings. PMDD is a more severe form of PMS characterized by increased symptom severity that peaks during the luteal phase and tends to improve or resolve shortly after...
421
Nephrotic Syndrome I : Introduction01:24

Nephrotic Syndrome I : Introduction

11
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...
11

You might also read

Related Articles

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

Sort by
Same author

Editorial: Comprehensive insights into microbial infection: from pathogenesis to therapeutic solutions.

Frontiers in cellular and infection microbiology·2026
Same author

Evidence for Drop-Like Nuclear Deformation in Sheared Endothelial Monolayers.

Small (Weinheim an der Bergstrasse, Germany)·2025
Same author

Inorganic Chiral Nanomaterials in Tissue Engineering Applications: Mini Review.

Tissue engineering. Part B, Reviews·2025
Same author

Non-melanin pigmentation: A narrative review.

Indian journal of dermatology, venereology and leprology·2025
Same author

Interpretable biophysical neural networks of transcriptional activation domains separate roles of protein abundance and coactivator binding.

bioRxiv : the preprint server for biology·2025
Same author

Prevalence of Sleep Disturbances in Rheumatoid Arthritis and Its Association With Disease Severity: A Hospital-Based Cross-Sectional Observation.

Cureus·2025

Related Experiment Video

Updated: Jul 30, 2025

Author Spotlight: Dermatopathology and the Treatment of Sexually Transmitted Diseases
04:25

Author Spotlight: Dermatopathology and the Treatment of Sexually Transmitted Diseases

Published on: November 8, 2024

1.8K

Herlyn-Werner-Wunderlich Syndrome: A Case Report.

Priyanka Vaidya1, Pooja Agarwal2, Achala Vaidya3

  • 1Department of Obstetrics and Gynaecology, Toowoomba Hospital, Toowoomba City QLD 4350, Queensland, Australia.

JNMA; Journal of the Nepal Medical Association
|May 19, 2023
PubMed
Summary

Herlyn-Werner-Wunderlich syndrome, a rare Mullerian and mesonephric duct anomaly, presents a diagnostic challenge. Early recognition of this triad is crucial for timely intervention and improved patient outcomes.

Area of Science:

  • Reproductive medicine
  • Gynecologic pathology
  • Congenital anomalies

Background:

More Related Videos

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

3.2K
A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
07:50

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

Published on: September 20, 2018

16.0K

Related Experiment Videos

Last Updated: Jul 30, 2025

Author Spotlight: Dermatopathology and the Treatment of Sexually Transmitted Diseases
04:25

Author Spotlight: Dermatopathology and the Treatment of Sexually Transmitted Diseases

Published on: November 8, 2024

1.8K
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

3.2K
A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts
07:50

A Metadata Extraction Approach for Clinical Case Reports to Enable Advanced Understanding of Biomedical Concepts

Published on: September 20, 2018

16.0K
  • Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly involving Mullerian and mesonephric duct development.
  • It is characterized by a triad: uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis.
  • Also known as obstructed hemivagina and ipsilateral renal anomaly, it often presents with nonspecific symptoms.