Related Experiment Video

Updated: Jun 9, 2026

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

Feline hypertrophic osteopathy: a collection of seven cases in Taiwan

Chiung-Hui Huang1, Chian-Ren Jeng, Chung-Tien Lin

  • 1Department of Veterinary Medicine, Graduate Institute of Veterinary Medicine and Veterinary Teaching Hospital, National Taiwan University, Number 1, Section 4, Roosevelt Road, Taipei City 106, Taiwan.

Journal of the American Animal Hospital Association
|September 3, 2010
PubMed

More Related Videos

Systematic Assessment of Mammalian Skull Specimens for Dental and Temporomandibular Joint Pathology07:26

Systematic Assessment of Mammalian Skull Specimens for Dental and Temporomandibular Joint Pathology

Published on: August 22, 2022

Tuina Intervention in Rabbit Model of Knee Osteoarthritis04:23

Tuina Intervention in Rabbit Model of Knee Osteoarthritis

Published on: August 25, 2023

Related Concept Videos

Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

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...