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

Signs of Puberty01:27

Signs of Puberty

1.2K
Puberty is a critical phase, typically beginning between the ages of 8 and 13 in girls and 9 and 14 in boys, though timing can vary based on genetics, environmental factors, and overall health. This period is characterized by the development of secondary sexual characteristics and the attainment of reproductive potential. Endocrine changes underpin puberty, with hormonal surges of Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH) instigated by Gonadotropin-Releasing Hormone (GnRH)...
1.2K
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

311
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...
311
Abnormal Proliferation02:23

Abnormal Proliferation

5.0K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.0K
The Mammary Glands01:12

The Mammary Glands

1.9K
The female breast is a hemispheric projection of variable size positioned anterior to the pectoralis major and serratus anterior muscles. A fascia layer composed of dense, irregular connective tissue connects it to these muscles.
Each breast features a pigmented projection known as the nipple, through which milk emerges via closely spaced openings of ducts, referred to as lactiferous ducts. Surrounding the nipple is a circular pigmented area of skin named the areola, which appears rough due to...
1.9K
Growth of Cartilage and Bone Tissue01:27

Growth of Cartilage and Bone Tissue

3.9K
Chondrocytes form a temporary cartilaginous model by dividing and secreting a thick gel-like extracellular matrix. Once the chondrocytes undergo programmed cell death, osteoblasts enter the site of the cartilaginous model. The process of replacing the temporary cartilaginous model with bone in an ordered manner is called endochondral ossification. In endochondral ossification, not all of the cartilage is replaced by bone tissue. Some cartilage that performs a protective and supportive function...
3.9K
Testes: Gross Anatomy01:19

Testes: Gross Anatomy

5.0K
The testes, also known as testicles, are the male gonads. They are housed within the scrotum, a sac-like structure located beneath the penis. The scrotum's primary role is to regulate the temperature of the testes, which is crucial for sperm production.
Each testis is surrounded by the tunica albuginea, a dense connective tissue layer that provides structural support and protection. This layer is covered by an outer serous membrane called the tunica vaginalis, which helps reduce friction...
5.0K

You might also read

Related Articles

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

Sort by
Same author

Indoor air exposure to brominated flame retardants in public primary schools and associations with childhood respiratory and skin outcomes.

Journal of hazardous materials·2026
Same author

CXCR3 signaling promotes Delta One T cell recruitment and antitumor efficacy in colorectal cancer.

Journal for immunotherapy of cancer·2026
Same author

The Largest Outbreak of Acute Gastroenteritis of Mixed Norovirus Genogroups in the Coast of São Paulo State, Brazil.

Viruses·2026
Same author

Central congenital hypothyroidism caused by <i>TSHB</i> gene mutation: a case report.

Journal of pediatric endocrinology & metabolism : JPEM·2026
Same author

Point prevalence of motor neuropathy in children and adolescents with type 1 diabetes mellitus.

Journal of diabetes and metabolic disorders·2026
Same author

Silent expansion: A case report of a young adult with ascending aortic aneurysm.

Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology·2025
Same journal

Clinical significance of miR-506-5p in type 2 diabetes mellitus and its regulatory effect on pancreatic β-cell proliferation.

Endokrynologia Polska·2026
Same journal

Comparative analysis of neuropsychological impairments between Cushing's disease and non-functioning pituitary adenoma patients: the roles of HPA axis hormones and inflammatory markers in a prospective cohort study.

Endokrynologia Polska·2026
Same journal

The influence of stress and cortisol on thyroid dysfunction.

Endokrynologia Polska·2026
Same journal

Serum adipocytokine levels in patients with renal cell carcinoma.

Endokrynologia Polska·2026
Same journal

The impact of cytopathologist-performed rapid on-site evaluation on the diagnostic adequacy of thyroid fine-needle aspiration.

Endokrynologia Polska·2026
Same journal

Partial lipodystrophy as a late complication of bone marrow transplantation for acute lymphoblastic leukemia.

Endokrynologia Polska·2026
See all related articles

Related Experiment Video

Updated: Dec 31, 2025

Ultrasonographic Evaluation of Breast Cancer-related Lymphedema
05:44

Ultrasonographic Evaluation of Breast Cancer-related Lymphedema

Published on: January 12, 2017

10.4K

Juvenile breast hypertrophy.

Benedita Bianchi de Aguiar1, Rita Santos Silva2, Carla Costa2

  • 1Paediatrics Department, Centro Hospital Entre Douro e Vouga, Santa Maria da Feira, Portugal. beneditabaguiar@gmail.com.

Endokrynologia Polska
|January 8, 2020
PubMed
Summary
This summary is machine-generated.

This study highlights the critical role of early detection and intervention in managing rare genetic disorders. Prompt diagnosis significantly improves patient outcomes and quality of life.

Keywords:
adolescentbreasthypertrophy

More Related Videos

Modeling Breast Cancer in Human Breast Tissue using a Microphysiological System
10:51

Modeling Breast Cancer in Human Breast Tissue using a Microphysiological System

Published on: April 23, 2021

4.5K
Integrating Augmented Reality Tools in Breast Cancer Related Lymphedema Prognostication and Diagnosis
06:03

Integrating Augmented Reality Tools in Breast Cancer Related Lymphedema Prognostication and Diagnosis

Published on: February 6, 2020

7.0K

Related Experiment Videos

Last Updated: Dec 31, 2025

Ultrasonographic Evaluation of Breast Cancer-related Lymphedema
05:44

Ultrasonographic Evaluation of Breast Cancer-related Lymphedema

Published on: January 12, 2017

10.4K
Modeling Breast Cancer in Human Breast Tissue using a Microphysiological System
10:51

Modeling Breast Cancer in Human Breast Tissue using a Microphysiological System

Published on: April 23, 2021

4.5K
Integrating Augmented Reality Tools in Breast Cancer Related Lymphedema Prognostication and Diagnosis
06:03

Integrating Augmented Reality Tools in Breast Cancer Related Lymphedema Prognostication and Diagnosis

Published on: February 6, 2020

7.0K

Area of Science:

  • Genetics
  • Pediatrics
  • Rare Diseases

Background:

  • Rare genetic disorders present diagnostic challenges due to their heterogeneity.
  • Early identification is crucial for timely and effective management.
  • Current diagnostic pathways can be lengthy and complex.

Observation:

  • A clinical vignette illustrating a rare genetic disorder was presented.
  • The case emphasized the importance of a multidisciplinary approach.
  • Diagnostic delays were noted as a significant barrier.

Findings:

  • The presented case underscores the need for increased awareness among healthcare professionals regarding rare genetic conditions.
  • Diagnostic tools and genetic testing play a pivotal role.
  • Timely intervention based on accurate diagnosis leads to improved therapeutic strategies.

Implications:

  • Enhanced diagnostic strategies for rare genetic disorders are essential.
  • Improved patient outcomes are achievable through early detection and tailored treatments.
  • Further research into novel diagnostic markers and therapeutic targets is warranted.