Neonatal teeth

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Neonatal teeth
Other namesNatal teeth
Specialty Dentistry

Natal teeth are teeth that are present above the gumline (have already erupted) at birth, and neonatal teeth are teeth that emerge through the gingiva during the first month of life (the neonatal period). [1] [2]

Contents

The incidence of neonatal teeth varies considerably, between 1:700 and 1:30,000 depending on the type of study; the highest prevalence is found in the only study that relies on personal examination of patients. [3]

Natal teeth, and neonatal teeth, can be the baby's normal deciduous teeth, sprouting prematurely. [4] These should be preserved, if possible. Alternately, they could be supernumerary teeth, extra teeth, not part of the normal allotment of teeth. [5]

Signs and symptoms

Most often natal teeth are mandibular central incisors. [6] They have little root structure and are attached to the end of the gum by soft tissue and are often mobile. [7]

Causes

Most of the time, natal teeth are not related to a medical condition. However, sometimes they may be associated with: [7]

Treatment

No intervention is usually recommended unless they are causing difficulty to the infant or mother. [3]

However some recommend that they be removed as the tooth can cut or amputate the tip of the tongue.

They should be left in the mouth as long as possible to decrease the likelihood of removing permanent tooth buds with the natal tooth. [9] They should also not be removed if the infant has hypoprothrombinemia. [9] In case of complications when the natal teeth need to be removed, dental radiographs should be obtained whenever possible, and evaluated and followed up with pediatric dentists. [9]

Notable cases

Related Research Articles

<span class="mw-page-title-main">Human tooth</span> Calcified whitish structure in humans mouths used to break down food

Human teeth function to mechanically break down items of food by cutting and crushing them in preparation for swallowing and digesting. As such, they are considered part of the human digestive system. Humans have four types of teeth: incisors, canines, premolars, and molars, which each have a specific function. The incisors cut the food, the canines tear the food and the molars and premolars crush the food. The roots of teeth are embedded in the maxilla or the mandible and are covered by gums. Teeth are made of multiple tissues of varying density and hardness.

<span class="mw-page-title-main">Hyperdontia</span> Condition of having extra teeth beyond the regular number of teeth

Hyperdontia is the condition of having supernumerary teeth, or teeth that appear in addition to the regular number of teeth. They can appear in any area of the dental arch and can affect any dental organ. The opposite of hyperdontia is hypodontia, where there is a congenital lack of teeth, which is a condition seen more commonly than hyperdontia. The scientific definition of hyperdontia is "any tooth or odontogenic structure that is formed from tooth germ in excess of usual number for any given region of the dental arch." The additional teeth, which may be few or many, can occur on any place in the dental arch. Their arrangement may be symmetrical or non-symmetrical.

Hypodontia is defined as the developmental absence of one or more teeth excluding the third molars. It is one of the most common dental anomalies, and can have a negative impact on function, and also appearance. It rarely occurs in primary teeth and the most commonly affected are the adult second premolars and the upper lateral incisors. It usually occurs as part of a syndrome that involves other abnormalities and requires multidisciplinary treatment.

<span class="mw-page-title-main">Ellis–Van Creveld syndrome</span> Medical condition

Ellis–Van Creveld syndrome is a rare genetic disorder of the skeletal dysplasia type.

<span class="mw-page-title-main">Ectodermal dysplasia</span> Group of genetic conditions affecting the embryonic ectoderm

Ectodermal dysplasia (ED) is a group of genetic syndromes all deriving from abnormalities of the ectodermal structures. More than 150 different syndromes have been identified.

<span class="mw-page-title-main">Human tooth development</span> Process by which teeth form

Tooth development or odontogenesis is the complex process by which teeth form from embryonic cells, grow, and erupt into the mouth. For human teeth to have a healthy oral environment, all parts of the tooth must develop during appropriate stages of fetal development. Primary (baby) teeth start to form between the sixth and eighth week of prenatal development, and permanent teeth begin to form in the twentieth week. If teeth do not start to develop at or near these times, they will not develop at all, resulting in hypodontia or anodontia.

<span class="mw-page-title-main">Malocclusion</span> Medical condition

In orthodontics, a malocclusion is a misalignment or incorrect relation between the teeth of the upper and lower dental arches when they approach each other as the jaws close. The English-language term dates from 1864; Edward Angle (1855-1930), the "father of modern orthodontics", popularised it. The word "malocclusion" derives from occlusion, and refers to the manner in which opposing teeth meet.

<span class="mw-page-title-main">Dentinogenesis imperfecta</span> Medical condition

Dentinogenesis imperfecta (DI) is a genetic disorder of tooth development. It is inherited in an autosomal dominant pattern, as a result of mutations on chromosome 4q21, in the dentine sialophosphoprotein gene (DSPP). It is one of the most frequently occurring autosomal dominant features in humans. Dentinogenesis imperfecta affects an estimated 1 in 6,000-8,000 people.

<span class="mw-page-title-main">Early childhood caries</span> Dental disease of young children

Early childhood caries (ECC), formerly known as nursing bottle caries, baby bottle tooth decay, night bottle mouth and night bottle caries, is a disease that affects teeth in children aged between birth and 71 months. ECC is characterized by the presence of 1 or more decayed, missing, or filled tooth surfaces in any primary tooth. ECC has been shown to be a very common, transmissible bacterial infection, usually passed from the primary caregiver to the child. The main bacteria responsible for dental caries are Streptococcus mutans and Lactobacillus. There is also evidence that supports that those who are in lower socioeconomic populations are at greater risk of developing ECC.

Anodontia is a rare genetic disorder characterized by the congenital absence of all primary or permanent teeth. It is divided into two subsections, complete absence of teeth or only some absence of teeth. It is associated with the group of skin and nerve syndromes called the ectodermal dysplasias. Anodontia is usually part of a syndrome and seldom occurs as an isolated entity. There is usually no exact cause for anodontia. The defect results in the dental lamina obstruction during embryogenesis due to local, systemic and genetic factors.

Dilaceration is a developmental disturbance in shape of teeth. It refers to an angulation, or a sharp bend or curve, in the root or crown of a formed tooth. This disturbance is more likely to affect the maxillary incisors and occurs in permanent dentition. Although this may seem more of an aesthetics issue, an impacted maxillary incisor will cause issues related to occlusion, phonetics, mastication, and psychology on young patients.

Macrodontia is a type of localized gigantism in which teeth are larger than normal. Macrodontia seen in permanent teeth is thought to affect around 0.03 to 1.9 percent of the worldwide population. Generally, patients with macrodontia have one or two teeth in their mouth that is abnormally large; however, single tooth growth is seen in a number of cases as well.

Dens evaginatus is a rare odontogenic developmental anomaly that is found in teeth where the outer surface appears to form an extra bump or cusp.

<span class="mw-page-title-main">Taurodontism</span> Molar condition in which the root is relatively short

Taurodontism is defined as the enlargement of pulp chambers with the furcation area being displaced toward the apex of the root of a tooth. It cannot be diagnosed clinically and requires radiographic visualization since the crown of a taurodontic tooth appears normal and its distinguishing features are present below the alveolar margin. Taurodontism can present in deciduous or permanent dentition, unilaterally or bilaterally, but is most common in the permanent molar teeth of humans. The underlying mechanism of taurodontism is the failure or late invagination of Hertwig's epithelial root sheath, which leads an apical shift of the root furcation.

Tooth gemination is a dental phenomenon that appears to be two teeth developed from one. There is one main crown with a cleft in it that, within the incisal third of the crown, looks like two teeth, though it is not two teeth. The number of the teeth in the arch will be normal.

<span class="mw-page-title-main">Talon cusp</span> Rare dental anomaly resulting in teeth having more than one cusp

Talon cusp is a rare dental anomaly resulting in an extra cusp or cusp-like projection on an anterior tooth, located on the inside surface of the affected tooth. Sometimes it can also be found on the facial surface of the anterior tooth.

<span class="mw-page-title-main">Dental attrition</span>

Dental attrition is a type of tooth wear caused by tooth-to-tooth contact, resulting in loss of tooth tissue, usually starting at the incisal or occlusal surfaces. Tooth wear is a physiological process and is commonly seen as a normal part of aging. Advanced and excessive wear and tooth surface loss can be defined as pathological in nature, requiring intervention by a dental practitioner. The pathological wear of the tooth surface can be caused by bruxism, which is clenching and grinding of the teeth. If the attrition is severe, the enamel can be completely worn away leaving underlying dentin exposed, resulting in an increased risk of dental caries and dentin hypersensitivity. It is best to identify pathological attrition at an early stage to prevent unnecessary loss of tooth structure as enamel does not regenerate.

<span class="mw-page-title-main">Enamel hypoplasia</span> Medical condition

Enamel hypoplasia is a defect of the teeth in which the enamel is deficient in quantity, caused by defective enamel matrix formation during enamel development, as a result of inherited and acquired systemic condition(s). It can be identified as missing tooth structure and may manifest as pits or grooves in the crown of the affected teeth, and in extreme cases, some portions of the crown of the tooth may have no enamel, exposing the dentin. It may be generalized across the dentition or localized to a few teeth. Defects are categorized by shape or location. Common categories are pit-form, plane-form, linear-form, and localised enamel hypoplasia. Hypoplastic lesions are found in areas of the teeth where the enamel was being actively formed during a systemic or local disturbance. Since the formation of enamel extends over a long period of time, defects may be confined to one well-defined area of the affected teeth. Knowledge of chronological development of deciduous and permanent teeth makes it possible to determine the approximate time at which the developmental disturbance occurred. Enamel hypoplasia varies substantially among populations and can be used to infer health and behavioural impacts from the past. Defects have also been found in a variety of non-human animals.

<span class="mw-page-title-main">Dental avulsion</span> Medical condition

Dental avulsion is the complete displacement of a tooth from its socket in alveolar bone owing to trauma. Normally, a tooth is connected to the socket by the periodontal ligament. When a tooth is knocked out, the ligament is torn.

Tooth ankylosis refers to a fusion between a tooth and underlying bony support tissues. In some species, this is a normal process that occurs during the formation or maintenance of the dentition. By contrast, in humans tooth ankylosis is pthological, whereby a fusion between alveolar bone and the cementum of a tooth occurs.

References

  1. Seminario, AL; Ivancaková, R (2004). "Natal and neonatal teeth". Acta Medica. 47 (4): 229–33. doi: 10.14712/18059694.2018.96 . PMID   15841901.
  2. Akash Ardeshana, Seema Bargale, Anuradha Karri, Bhavna Dave (January–March 2016). "Dentitia Praecox - Natal Teeth: A Case Report and Review" (PDF). Journal of Applied Dental and Medical Sciences . Vol. 2, no. 1. Retrieved 2018-11-08. Exact etiology for this condition is unknown. Different factors like heredity, environmental toxicant, endocrine disturbances, and superficial position of tooth germ are associated with etiology{{cite news}}: CS1 maint: multiple names: authors list (link)
  3. 1 2 MASSLER, M; SAVARA, BS (March 1950). "Natal and neonatal teeth; a review of 24 cases reported in the literature". The Journal of Pediatrics. 36 (3): 349–59. doi:10.1016/S0022-3476(50)80105-1. PMID   15405415.
  4. Vishal Khandelwal; Ullal Anand Nayak; Prathibha Anand Nayak; Yash Bafna (2013-06-02). "Management of an infant having natal teeth". BMJ Case Rep. 2013: bcr2013010049. doi:10.1136/bcr-2013-010049. PMC   3703024 . PMID   23737593. If the erupted tooth is diagnosed as a tooth of the normal dentition, each of the other situations mentioned above should be considered. It also avoids future space management issues. The maintenance of these teeth in the mouth is the first treatment option, unless this would cause injury to the baby.
  5. 1 2 3 4 5 6 7 8 9 Alexander K.C. Leung, William Lane M. Robson (2006). "Natal Teeth: A Review". Journal of the National Medical Association . 98 (2): 226–8. PMC   2595049 . PMID   16708508. Historical figures, such as Richard III, Louis XIV, Napoleon, Mirabeau, Mazarin, Cardinal Richelieu, Zoroaster and Hannibal, were described as examples of the former.
  6. Kates, GA; Needleman, HL; Holmes, LB (September 1984). "Natal and neonatal teeth: a clinical study". Journal of the American Dental Association. 109 (3): 441–3. doi:10.14219/jada.archive.1984.0415. PMID   6592231.
  7. 1 2 3 4 5 6 "Natal teeth". MedlinePlus : U.S. National Library of Medicine. Retrieved 7 April 2013.
  8. "Ellis-van Creveld syndrome". MedlinePlus : U.S. National Library of Medicine. Retrieved 7 April 2013.
  9. 1 2 3 Martinez, CR (March 1978). "Management of natal teeth". The Journal of Family Practice. 6 (3): 654–5. PMID   632777.
  10. 1 2 3 4 Berkovitz, Barry K.B (2012). Nothing but the Tooth: A Dental Odyssey. Newnes. p. 12. ISBN   978-0-12-397193-7 . Retrieved 8 July 2014.
  11. Fallon, Kevin (April 28, 2015). "Kate Mulgrew Bares Her Teeth". The Daily Beast. Retrieved May 1, 2015.