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Type IV Collagen of Basal Lamina01:05

Type IV Collagen of Basal Lamina

Type IV collagen is a 400 nm long, network-forming collagen that acts as a barrier between the epithelial and endothelial cells. Type IV collagen  forms the backbone of the basement membrane by scaffolding with laminin, entactin, proteoglycans, and fibronectin. Apart from rendering structural support to the basement membrane, it also helps entail signaling potentials necessary for both pathological and physiological functions.
A type IV collagen molecule has six alpha chains which can exist in...
Fibril-associated Collagen01:11

Fibril-associated Collagen

Fibril-associated collagens are a type of collagens present in the extracellular matrix with interrupted triple helices or FACIT (Fibril-associated collagens interrupted triple-helices). FACIT help connect and attach the collagen fibrils with each other as well as with other proteins of the extracellular matrix.
For example, the type II collagen fibrils in cartilage have covalently bound type IX fibril-associated collagens at regular intervals. Other types of fibril-associated collagens are...
Rheumatic Heart Disease I: Introduction01:23

Rheumatic Heart Disease I: Introduction

Rheumatic heart disease or RHD is a chronic condition that results from rheumatic fever, causing permanent damage to the heart valves.Etiology and Risk FactorsIt primarily arises from rheumatic fever, an inflammatory disease that can develop after untreated or inadequately treated group A streptococcal (GAS) pharyngitis. Streptococcus spreads through direct contact with oral or respiratory secretions. While the bacteria are the causative agents, factors like malnutrition, overcrowding, poor...
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
Cirrhosis II: Pathophysiology01:24

Cirrhosis II: Pathophysiology

Cirrhosis is a progressive chronic liver injury caused by prolonged inflammation, excessive fibrotic remodeling, and impaired regeneration. Over time, repeated hepatic insults disrupt the liver’s architecture and function, leading to reduced blood flow, impaired bile drainage, and diminished metabolic capacity.Pathophysiology of cirrhosisCirrhosis arises from three main responses to chronic liver damage: inflammation, immune activation, and hepatocyte death. These processes lead to structural...
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Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
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Related Experiment Video

Updated: Jun 16, 2026

Preparing Porcine Eyes for Confocal Reflectance Microscopy to Visualize the Vitreous Collagen Fiber Network
06:07

Preparing Porcine Eyes for Confocal Reflectance Microscopy to Visualize the Vitreous Collagen Fiber Network

Published on: October 17, 2025

Familial reactive perforating collagenosis.

Yasmeen J Bhat1, Sheikh Manzoor, Seema Qayoom

  • 1Department of Dermatology, STD & Leprosy, SKIMS Medical College Hospital, Srinagar, India. yasmeen_bhat2001@yahoo.co.in

Indian Journal of Dermatology
|January 27, 2010
PubMed
Summary
This summary is machine-generated.

Reactive perforating collagenosis (RPC) is a rare genetic skin disorder typically starting in childhood. Combination therapy with oral and topical retinoids alongside emollients offers the best treatment outcome.

Keywords:
Familialretinoidstransepidermal eliminationumbilicated

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Area of Science:

  • Dermatology
  • Genetics
  • Pathology

Background:

  • Reactive perforating collagenosis (RPC) is a rare genodermatosis characterized by transepidermal elimination of abnormal collagen.
  • Typically presents in early childhood with asymptomatic, umbilicated papules on extremities that worsen with age.

Purpose of the Study:

  • To elucidate the clinico-pathological characteristics of RPC.
  • To evaluate the efficacy of diverse treatment strategies for RPC.

Main Methods:

  • Clinical assessment of ten RPC patients from five families.
  • Histopathological examination for diagnosis.
  • Administration of various topical and oral therapeutic agents.

Main Results:

  • RPC often exhibits a familial pattern, though inheritance is not clearly defined.
  • Disease onset in childhood with recurrent, progressively enlarging lesions.
  • No correlation found between systemic diseases and RPC onset.

Conclusions:

  • Combined oral and topical retinoids with emollients represent the optimal therapeutic approach for RPC.