Get Even More Visitors To Your Blog, Upgrade To A Business Listing >>

Oligodontia | Causes, Diagnosis and Treatments

Oligodontia | Causes, Diagnosis and Treatments

Introduction

The most prevalent developmental anomaly in humans is dental agenesis, which frequently poses a serious clinical issue, It is classified based on the number of missing permanent Teeth, excluding third molars. We will discuss Oligodontia in this article.

The term hypodontia refers to the absence of one or more teeth.

Oligodontia refers to the absence of multiple teeth (more than six teeth), excluding the third molars.

Anodontia is an extreme form of oligodontia in which all dental structure is absent.

In permanent dentition, the population prevalence is 0.3%.

It can occur alone, as part of a syndrome, or in more serious systemic disturbances such as ectodermal dysplasia.

If oligodontia is part of a syndrome, there are usually changes to the skin, nails, eyes, ears, or skeleton.

It is an integral part of more than 120 syndromes.

Hypodontia oligodontia and anodontia defined according of the number of missing teeth

Causes of Oligodontia

Generally, tooth agenesis may be caused by: –

  • Local trauma.
  • Chemotherapy.
  • Radiotherapy.
  • It can occur as part of a systemic genetic syndrome or as an independent oral trait linked to mutations in multiple genes.

Other Causes Include: –

  • Viral disease during pregnancy.
  • Metabolic imbalances.
  • Developmental abnormalities.
  • Environmental factors
  • Autosomal dominant mutations in PAX9 and MSX1 have been found in patients with molar non-syndromic oligodontia.

The most recent gene found to be responsible for oligodontia is an autosomal recessive mutation in LTBP3, the gene that encodes latent TGF-b binding protein 3, an extracellular matrix protein thought to be necessary for osteoclast function.

Diagnosis of Oligodontia

When teeth are suspected to be missing, a clinical examination is conducted along with a panoramic radiograph (and intra-oral X-rays if needed).

Oligodontia is suggested by the delayed eruption of teeth, persistence of primary teeth, alveolar bone hypotrophy, and the presence of diastemas.

Normally, all primary teeth and the crypts of the first permanent molars are visible on radiographs at birth, and the crowns of the permanent teeth (except third molars) at 6 years of age.

A diagnosis of oligodontia is made when there are more than six missing teeth.

Treatment of Oligodontia

Persons with tooth agenesis currently have a variety of treatment options.

Generally, the replacement of lost or deficient tissues is based on drug therapies, the use of different prosthetic materials and implants, and tissue/organ transplantations.

Synthetic dental implants are a common standard procedure for replacing missing teeth, and their success has grown in recent decades.

Different fixtures, including implants, crowns, bridges, fixed or removable, complete and partial dentures, have proven to be sufficient over time.

The undesirable outcomes include a potential infection-causing failure of the implant to integrate with the bone, leading to implant loss and potential bone loss.

Implants placed in developing alveolar ridges have been shown to inhibit ridge formation.

Summary

The most prevalent developmental anomaly in humans is dental agenesis, which frequently poses a serious clinical issue.

It is classified based on the number of missing permanent teeth, excluding third molars.

Oligodontia refers to the absence of multiple teeth (more than six teeth), excluding the third molars.

If oligodontia is part of a syndrome, there are usually changes to the skin, nails, eyes, ears, or skeleton.

The most recent gene found to be responsible for oligodontia is an autosomal recessive mutation in LTBP3, the gene that encodes latent TGF-b binding protein 3, an extracellular matrix protein thought to be necessary for osteoclast function.

When teeth are suspected to be missing, a clinical examination is conducted along with a panoramic radiograph (and intra-oral X-rays if needed).

Oligodontia is suggested by the delayed eruption of teeth, persistence of primary teeth, alveolar bone hypotrophy, and the presence of diastemas.

Persons with tooth agenesis currently have a variety of treatment options.

Generally, the replacement of lost or deficient tissues is based on drug therapies, the use of different prosthetic materials and implants, and tissue/organ transplantations.

Synthetic dental implants are a common standard procedure for replacing missing teeth, and their success has grown in recent decades.

How useful was this post?

Click on a star to rate it!

Average rating 0 / 5. Vote count: 0

No votes so far! Be the first to rate this post.

As you found this post useful...

Keep in touch on social media!

I'm sorry that this post was not useful for you!

Let me improve this post!

Tell me how I can improve this post?

References

  1. Oligodontia: Case report and review of literature – researchgate. Retrieved December 5, 2022, from ResearchGate
  2. Hypodontia, Oligodontia, and Anodontia defined according of the number … (n.d.). Retrieved December 5, 2022, from ResearchGate
  3. Nonsyndromic Oligodontia in permanent dentition: Three rare cases. (n.d.). Retrieved December 5, 2022, from ResearchGate
  4. Orphanet: Oligodontia. Retrieved December 5, 2022, from Orphanet
 
 

Featured Posts

Herbal Medicine, Benefits, Importance, and Risks

Herbal medicine is the use of a plant's seeds, berries, roots, leaves, bark, or flowers for medicinal purposes. Many people mistakenly believe that products labeled "natural" are always safe and beneficial to their health.
Read more

12 Natural Remedies for Psoriasis You Should Know

Natural remedies become an effective psoriasis treatment, with lower costs and fewer side- or toxic effects than other therapies.
Read more

Anemia | Types, Causes, Symptoms, and Treatments

Anemia is defined as a reduction in the amount of red blood cells or hemoglobin in the circulation. It is a common nutritional deficiency disorder and a global public health problem.
Read more

Recent Posts

Types of Hazards in Occupational Health

Workplace hazards can be classified into five broad categories. These hazards can cause an immediate or delayed response, depending on their inherent characteristics as well as the intensity and frequency of exposure.
Read more

Chronic Abdominal Pain | Causes, Symptoms and Treatments

Oligodontia | Causes, Diagnosis and Treatments

Waste Control | 8 Strategies and Practices

Popular Posts

  • Types of Hazards in Occupational Health

  • Chronic Abdominal Pain | Causes, Symptoms and Treatments

  • Oligodontia | Causes, Diagnosis and Treatments

  • Waste Control | 8 Strategies and Practices

  • Hemolytic Anemia | Causes, Symptoms and Treatments

  • Ultimate Guide to FAQs About Anemia +20 Qs

  • Alcoholism and Anemia | Overview

  • Microcytic Anemia | Types, Diagnosis and Treatments

  • Macrocytic Anemia | Causes, Signs, Symptoms and Treatments

  • How Does Chronic Pain Affect the Brain

  • Psychological Effects of Chronic Pain

  • What Not To Eat When You Are Anemic?

  • Netherton Syndrome

  • What Decreases Iron Absorption?

  • 13 Common Home Remedies for Toothache and How to Use

  • Iron Deficiency Anemia Causes, Symptoms and Treatments

  • 12 Natural Remedies for Psoriasis You Should Know

  • Herbal Medicine, Benefits, Importance, and Risks

  • Iron Rich Foods | Everything About Iron

  • Medications for Anemia and Nutritional Treatments

  • Blood Disorders List

  • Megaloblastic Anemia

  • Anemia of Chronic Disease

  • Occupational Health: All You Need To Know

  • Anemia and COVID-19

  • Iron Deficiency Anemia and Anxiety

  • Anemia and Menstruation | Causes and Treatments

  • Anemia | Types, Causes, Symptoms, and Treatments

Learn More

Occupational Health

Types of Hazards in Occupational Health

Chronic Pain

Chronic Abdominal Pain | Causes, Symptoms and Treatments

Developmental anomalies

Oligodontia | Causes, Diagnosis and Treatments

Environmental Health

Waste Control | 8 Strategies and Practices

[spt-posts-ticker]

Netherton Syndrome

Netherton Syndrome is a rare hereditary autosomal recessive multisystem disorder characterized by generalized erythroderma at birth or...



This post first appeared on Medicaregate, please read the originial post: here

Share the post

Oligodontia | Causes, Diagnosis and Treatments

×

Subscribe to Medicaregate

Get updates delivered right to your inbox!

Thank you for your subscription

×