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

Lysosomal Hydrolases01:22

Lysosomal Hydrolases

4.7K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
4.7K
Overview of Lipid Metabolism01:24

Overview of Lipid Metabolism

6.6K
Lipid metabolism is a crucial process in the human body that involves the synthesis and degradation of lipids. This process is essential for energy production, cell membrane formation, and hormone production, among other functions.
Lipolysis: The Breakdown of Lipids:
Lipolysis is the process of breaking down lipids, particularly triglycerides, into glycerol and fatty acids. This process typically occurs in the adipose tissue and is triggered by various hormones, including glucagon and...
6.6K
Protein Import into the Peroxisomes01:27

Protein Import into the Peroxisomes

5.6K
Cells contain membrane-bound organelles called peroxisomes that oxidize organic molecules by transferring hydrogen atoms to oxygen, producing hydrogen peroxide. Peroxisomes enzymatically convert the released hydrogen peroxide into water and oxygen.
Peroxisomal Protein Import:
Peroxisomes lack the genetic machinery required to code for their own proteins. Hence, most peroxisomal membrane, lumenal and transmembrane proteins are synthesized in the cytoplasm or ER and transported to the peroxisome...
5.6K
Blood Studies for Cardiovascular System III: Serum Lipid Profile01:25

Blood Studies for Cardiovascular System III: Serum Lipid Profile

793
Understanding serum lipids is crucial for maintaining cardiovascular health and preventing heart disease and stroke.
Serum lipids are fats and fatty substances in the blood and are crucial for various bodily functions, including energy storage, cellular structure, and hormone production. Serum lipids consist of cholesterol, triglycerides, and phospholipids.
Cholesterol is a soft, fat-like substance found in all body cells. It is crucial for producing hormones, vitamin D, and substances that aid...
793
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

4.6K
Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
4.6K
Nephrotic Syndrome I : Introduction01:24

Nephrotic Syndrome I : Introduction

897
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...
897

You might also read

Related Articles

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

Sort by
Same author

Efficacy and Safety of Imsidolimab for Generalized Pustular Psoriasis.

NEJM evidence·2026
Same author

Optical Coherence Tomography Findings in Patients With Psoriasis: Reduced Choroidal Vascularity Index.

International journal of dermatology·2026
Same author

Dysmenorrhea in Chronic Spontaneous Urticaria: A Subset of Patients Report Worsening and Partial Antihistamine Benefit: UCARE HURDLE-I Study.

International journal of dermatology·2025
Same author

The interaction between the Mediterranean diet, obesity, and disease severity: A case-control study on psoriatic patients.

Nutrition and health·2025
Same author

Is There a Relationship Between Serum BDNF Levels, Disease Severity, and Psychiatric Symptoms in Adolescents with Atopic Dermatitis?

Children (Basel, Switzerland)·2025
Same author

Pigmented Purpuric Dermatosis Following Tumor Necrosis Factor-Alpha Inhibitor Therapy: A Case Report.

Archives of rheumatology·2025

Related Experiment Video

Updated: Mar 23, 2026

Author Spotlight: Analysis of Fluorescent-Stained Lipid Droplets with 3D Reconstruction for Hepatic Steatosis Assessment
07:12

Author Spotlight: Analysis of Fluorescent-Stained Lipid Droplets with 3D Reconstruction for Hepatic Steatosis Assessment

Published on: June 2, 2023

8.9K

Lipoid proteinosis.

Demet Kartal1, Salih Levent Çınar1, Levent Kartal2

  • 1Department of Dermatology and Venereology, Erciyes University Faculty of Medicine, Kayseri, Turkey.

Acta Dermatovenerologica Alpina, Pannonica, Et Adriatica
|March 26, 2016
PubMed
Summary
This summary is machine-generated.

Lipoid proteinosis (LP) is a rare genetic disorder. This case highlights significant oral mucosal issues in an LP patient, differing from typical skin-predominant symptoms.

More Related Videos

Author Spotlight: Evaluation of Lipid Droplet Size and Fusion in Bovine Hepatic Cells
08:37

Author Spotlight: Evaluation of Lipid Droplet Size and Fusion in Bovine Hepatic Cells

Published on: March 10, 2023

3.5K
Rapid Lipid Droplet Isolation Protocol Using a Well-established Organelle Isolation Kit
08:43

Rapid Lipid Droplet Isolation Protocol Using a Well-established Organelle Isolation Kit

Published on: April 19, 2019

12.4K

Related Experiment Videos

Last Updated: Mar 23, 2026

Author Spotlight: Analysis of Fluorescent-Stained Lipid Droplets with 3D Reconstruction for Hepatic Steatosis Assessment
07:12

Author Spotlight: Analysis of Fluorescent-Stained Lipid Droplets with 3D Reconstruction for Hepatic Steatosis Assessment

Published on: June 2, 2023

8.9K
Author Spotlight: Evaluation of Lipid Droplet Size and Fusion in Bovine Hepatic Cells
08:37

Author Spotlight: Evaluation of Lipid Droplet Size and Fusion in Bovine Hepatic Cells

Published on: March 10, 2023

3.5K
Rapid Lipid Droplet Isolation Protocol Using a Well-established Organelle Isolation Kit
08:43

Rapid Lipid Droplet Isolation Protocol Using a Well-established Organelle Isolation Kit

Published on: April 19, 2019

12.4K

Area of Science:

  • Dermatology
  • Genetics
  • Otolaryngology

Background:

  • Lipoid proteinosis (LP) is an uncommon autosomal recessive disorder.
  • Characterized by hoarseness, waxy papules, acneiform scarring, and eyelid beading.
  • Typically presents with cutaneous manifestations.

Observation:

  • A 42-year-old woman presented with oral mucosa rigidity and limited tongue movement.
  • She experienced burning sensation, decreased taste, and hoarseness.
  • Diagnosed with lipoid proteinosis.

Findings:

  • The patient exhibited significant oral mucosal involvement.
  • Cutaneous manifestations were less pronounced than typically observed.
  • This case presents an atypical phenotype of lipoid proteinosis.

Implications:

  • Highlights the variability of lipoid proteinosis presentation.
  • Emphasizes the importance of considering mucosal involvement in LP diagnosis.
  • Suggests further research into genotype-phenotype correlations in lipoid proteinosis.