What syndromes are associated with oligodontia?

Oligodontia can occur in association with various genetic syndromes

genetic syndromes

When the genetic disorder is inherited from one or both parents, it is also classified as a hereditary disease. Some disorders are caused by a mutation on the X chromosome and have X-linked inheritance. Very few disorders are inherited on the Y chromosome or mitochondrial DNA (due to their size).

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Genetic disorder - Wikipedia

, like ectodermal dysplasia, Van Der Woude syndrome, Down syndrome and Reiger syndrome or as a nonsyndromic

nonsyndromic

Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of nonsyndromic deafness.

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Nonsyndromic deafness - Wikipedia

isolated familial trait, or as an infrequent finding.

What genetic or congenital conditions are associated with hypodontia or oligodontia?

EDA, EDAR and EDARADD genes are indeed responsible both for isolated or syndromic hypo/oligodontia. Many other genes are involved in hypo/oligodontia such as MSX1, PAX9, IRF6, GREM2, AXIN2, LRP6, SMOC2, LTBP3, PITX2, and WNT10B.

What causes oligodontia?

Possible causes of oligodontia include viral disease during pregnancy, genetic predisposition, metabolic imbalances, developmental abnormalities and environmental factors. Autosomal dominant mutations in PAX9 and MSX1 have been found in patients with molar non-syndromic oligodontia.

What type of mutation causes oligodontia?

WNT10A mutations are the most commonly reported in the genetic etiology for syndromic oligodontia and PAX9 mutations are the most commonly reported genetic etiology for isolated oligodontia. Oligodontia is not only a disorder of missing teeth but also a clinical sign of a potentially complex systemic condition.

Is oligodontia a disability?

Conclusions: Oligodontia is a heterogeneous condition. Patients with oligodontia can be classified as having three different types according to the extent of their disability and the complexity of their prosthodontic requirements.

Hypodontia | Anodontia | Oligodontia | Developmental disturbances of teeth | Dr Paridhi Agrawal

Is anodontia hereditary?

Anodontia is an inherited genetic defect. The exact genes involved are unknown. However, Anodontia is usually associated with ectodermal dysplasia. Ectodermal dysplasia is not one disorder but a group of closely related hereditary conditions that affect the hair, nails, skin, and sweat glands.

How common is anodontia?

The prevalence of anodontia is unknown but it is a very rare disorder. Anodontia occurs in less than 2-8% of the general population in regards to permanent teeth and 0.1-0.7% in primary teeth.

How is oligodontia inherited?

Genetic Causes

If one or both of your parents experience a genetic disorder or mutation, it's not a guarantee that you will develop the same condition. Genetic causes are varied, given that oligodontia is caused by both genetic syndromes and inherited family traits.

What is Dentinogenesis imperfecta?

Dentinogenesis imperfecta is a disorder of tooth development. This condition causes the teeth to be discolored (most often a blue-gray or yellow-brown color) and translucent.

What is ectodermal dysplasia caused by?

The different types of ectodermal dysplasia are caused by the mutation or deletion of certain genes located on different chromosomes. Because ectodermal dysplasias are caused by a genetic defect they may be inherited or passed down the family line.

What is ectodermal dysplasia syndrome?

The ectodermal dysplasias (EDs) are a heterogeneous group of nearly 100 inherited disorders characterized by anomalies in at least two of the structures derived from the embryonic ectoderm, with at least one involving the skin appendages (hair, nails, sweat glands) or teeth.

What is pseudo anodontia?

Pseudoanodontia is a descriptive term that indicates clinical but not radiographic absence of teeth that should normally be present in the oral cavity for the patient's dental and chronologic age.

What are the commonest congenitally missing teeth?

The most common congenitally missing teeth are wisdom teeth, upper lateral incisors, and the second premolars(source).

What is Amelogenesis imperfecta?

Amelogenesis imperfecta (AI) refers to a group of rare, inherited disorders characterized by abnormal enamel formation. The term is typically restricted to those disorders of enamel development not associated with other abnormalities of the body.

What is Turner's hypoplasia?

Turner's Tooth, also called Enamel Hypoplasia by professionals in the field, is a condition that reduces a tooth's enamel thickness, increases tooth sensitivity, leaves the affected tooth more susceptible to decay, and results in an unsightly appearance.

What is Talon cusp?

Talon cusp is a rare dental anomaly in which a cusp-like mass of hard tissue protrudes from the cingulum area of maxillary or mandibular anterior teeth. The typical appearance of this projection is conical and resembles an eagle's talon.

What is Microdontia?

Microdontia refers to teeth that are smaller than normal, whereas macrodontia (megadontia) relates to teeth that are larger than normal.

What is Turner's tooth?

An enamel defect in the permanent teeth caused by periapical inflammatory disease in the overlying primary tooth is referred to as Turner's tooth (also known as Turner's hypoplasia).

What is cause Hypercementosis?

Hypercementosis is excessive deposition of cementum on the tooth roots. In most cases, its cause is unknown. Occasionally, it appears on a supraerupted tooth after the loss of an opposing tooth. Another cause of hypercementosis is inflammation, usually resulting from rarefying or sclerosing osteitis.

Is having no teeth a disability?

Therefore, an individual should be considered to have a dental disability if orofacial pain, infection, or pathological condition and/or lack of functional dentition affect nutritional intake, growth and development, or participation in life activities.

What is the second tooth in hypodontia?

The second premolars – these are the teeth right in front of your molars. One may sometimes be removed during braces treatment, but if your child is missing this permanent tooth, chances are it's due to hypodontia.

What causes severe hypodontia?

Hypodontia is usually the result of a problem with the band of tissue under the gums (dental lamina) where the teeth form. The most common cause of these problems is heredity or family history. A mutation of one of the specific genes which help form the dental lamina properly can lead to hypodontia.

What is the difference between anodontia and hypodontia?

Hypodontia refers to the absence of fewer than 6 teeth (not including third molars). Oligodontia refers to the absence of 6 or more teeth (not including third molars). Anodontia is the complete absence of teeth. Hypodontia is more common in the permanent dentition than in the primary dentition.

What is false anodontia?

Definition. Absence of teeth as a result of impaction, delayed eruption, exfoliation or extraction. [

Are peg laterals hereditary?

Peg-shaped teeth are a hereditary dental disorder called microdontia, a condition where one or more teeth appear smaller than average (microdontia) [1]. In general, the most common teeth affected are the upper lateral incisors or sometimes third molars.