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Related Concept Videos

Bone Formation by Endochondral Ossification01:24

Bone Formation by Endochondral Ossification

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Bone formation, or ossification, begins around the sixth to seventh week of embryonic development. Most bones develop from a cartilaginous template through the process of endochondral ossification. Cartilage formation begins when clusters of mesenchymal cells differentiate into chondrocytes. These chondrocytes proliferate rapidly and secrete an extracellular matrix that becomes encased in a membrane called the perichondrium. The resulting cartilage model provides a template that resembles the...
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Bone Disorders01:29

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Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
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Bone Formation by Intramembranous Ossification01:29

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Intramembranous ossification is one of the two processes involved in the development of bones within an embryo. The flat bones of the face, most of the cranial bones, and the clavicles are formed via this process. During intramembranous ossification, the bones develop directly from sheets of undifferentiated mesenchymal connective tissue.
The process begins when mesenchymal cells in the embryonic skeleton gather together and differentiate into osteogenic cells, which then develop into ...
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Bone Remodeling and Repair01:31

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Spongy Bone01:09

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All bones comprise an outer layer of compact bone, and an interior made up of spongy bone tissue, also called cancellous or trabecular bone. In long bones, spongy bone tissue is mainly found in the interior of the epiphyses (broad ends of the bone).
Spongy bone is more porous, and less dense compared to compact bone. It is composed of concentric lamellae that are arranged irregularly to form the trabecular network. In some bones, the spaces between trabeculae contain red marrow, where...
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Fractures: Bone Repair01:27

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Treatment for a fracture is based on the type of break, the bone affected, and the patient's age.
Minor fractures with no bone displacement are treated by immobilizing the fractured bone using a cast or splint. However, in the case of fractures with displaced bones, the broken bones are repositioned before immobilization to ensure successful healing without deformation and loss of function. The realignment of fractured bone ends is performed through a process called reduction. If the...
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Related Experiment Video

Updated: Mar 25, 2026

Direct Mouse Trauma/Burn Model of Heterotopic Ossification
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Fibrodysplasia Ossificans Progressiva.

Usman Rashid1, Attia Bari1, Amna Maqsood1

  • 1Department of Pediatric Medicine, Children Hospital and Institute of Child Health, Lahore.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|February 16, 2016
PubMed
Summary

Fibrodysplasia Ossificans Progressiva (FOP) is a rare genetic disorder causing bone to form in soft tissues. This case study details a 3-year-old boy with FOP, highlighting his progressive symptoms and ossification.

Area of Science:

  • Medical Genetics
  • Rare Diseases
  • Skeletal Biology

Background:

  • Fibrodysplasia Ossificans Progressiva (FOP) is a rare genetic disorder.
  • Characterized by progressive heterotopic ossification and congenital hallux valgus.

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  • Autosomal dominant inheritance pattern.