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Advanced eruption of teeth

MedGen UID:
78588
Concept ID:
C0266054
Finding
Synonyms: Premature eruption of teeth; Premature tooth eruption
SNOMED CT: Premature tooth eruption (16000003); Precocious dentition (16000003); Accelerated tooth eruption (16000003); Precocious tooth eruption (16000003)
 
HPO: HP:0006288

Definition

Premature tooth eruption, which can be defined as tooth eruption more than 2 SD earlier than the mean eruption age. [from HPO]

Term Hierarchy

Conditions with this feature

Sotos syndrome
MedGen UID:
61232
Concept ID:
C0175695
Disease or Syndrome
Sotos syndrome is characterized by a distinctive facial appearance (broad and prominent forehead with a dolichocephalic head shape, sparse frontotemporal hair, downslanting palpebral fissures, malar flushing, long and narrow face, long chin); learning disability (early developmental delay, mild-to-severe intellectual impairment); and overgrowth (height and/or head circumference =2 SD above the mean). These three clinical features are considered the cardinal features of Sotos syndrome. Major features of Sotos syndrome include behavioral problems (most notably autistic spectrum disorder), advanced bone age, cardiac anomalies, cranial MRI/CT abnormalities, joint hyperlaxity with or without pes planus, maternal preeclampsia, neonatal complications, renal anomalies, scoliosis, and seizures.
Rabson-Mendenhall syndrome
MedGen UID:
78783
Concept ID:
C0271695
Disease or Syndrome
INSR-related severe syndromic insulin resistance comprises a phenotypic spectrum that is a continuum from the severe phenotype Donohue syndrome (DS) (also known as leprechaunism) to the milder phenotype Rabson-Mendenhall syndrome (RMS). DS at the severe end of the spectrum is characterized by severe insulin resistance (hyperinsulinemia with associated fasting hypoglycemia and postprandial hyperglycemia), severe prenatal growth restriction and postnatal growth failure, hypotonia and developmental delay, characteristic facies, and organomegaly involving heart, kidneys, liver, spleen, and ovaries. Death usually occurs before age one year. RMS at the milder end of the spectrum is characterized by severe insulin resistance that, although not as severe as that of DS, is nonetheless accompanied by fluctuations in blood glucose levels, diabetic ketoacidosis, and – in the second decade – microvascular complications. Findings can range from severe growth delay and intellectual disability to normal growth and development. Facial features can be milder than those of DS. Complications of longstanding hyperglycemia are the most common cause of death. While death usually occurs in the second decade, some affected individuals live longer.
Malan overgrowth syndrome
MedGen UID:
766574
Concept ID:
C3553660
Disease or Syndrome
Malan syndrome (MALNS) is clinically characterized by overgrowth, advanced bone age, macrocephaly, and dysmorphic facial features. Patients develop marfanoid habitus, with long and slender body, very low body mass, long narrow face, and arachnodactyly, with age. Impaired intellectual development and behavior anomalies are present (summary by Martinez et al., 2015).
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
MedGen UID:
862975
Concept ID:
C4014538
Disease or Syndrome
ADNP-related disorder is characterized by hypotonia, severe speech and motor delay, mild-to-severe intellectual disability, and characteristic facial features (prominent forehead, high anterior hairline, wide and depressed nasal bridge, and short nose with full, upturned nasal tip) based on a cohort of 78 individuals. Features of autism spectrum disorder are common (stereotypic behavior, impaired social interaction). Other common findings include additional behavioral problems, sleep disturbance, brain abnormalities, seizures, feeding issues, gastrointestinal problems, visual dysfunction (hypermetropia, strabismus, cortical visual impairment), musculoskeletal anomalies, endocrine issues including short stature and hormonal deficiencies, cardiac and urinary tract anomalies, and hearing loss.
Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features
MedGen UID:
1647077
Concept ID:
C4693405
Disease or Syndrome
Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features (NEDMAGA) is characterized by infantile-onset global developmental delay with severe to profound intellectual disability, mildly delayed walking with broad-based and unsteady gait, and absence of meaningful language. Patients have features of autism, with repetitive behaviors and poor communication, but usually are socially reactive and have a happy demeanor. More variable neurologic features include mild seizures, spasticity, and peripheral neuropathy (summary by Palmer et al., 2017).
Chromosome 13q33-q34 deletion syndrome
MedGen UID:
1744234
Concept ID:
C5436890
Disease or Syndrome
Chromosome 13q33-q34 deletion syndrome is associated with developmental delay and/or impaired intellectual development, facial dysmorphism, and an increased risk for epilepsy, cardiac defects and additional anatomic anomalies (summary by Sagi-Dain et al., 2019).

Professional guidelines

PubMed

Goldstein G, Goodacre C, MacGregor K
J Prosthodont 2021 Apr;30(S1):12-19. doi: 10.1111/jopr.13315. PMID: 33783090
Vuorimies I, Arponen H, Valta H, Tiesalo O, Ekholm M, Ranta H, Evälahti M, Mäkitie O, Waltimo-Sirén J
Bone 2017 Jan;94:29-33. Epub 2016 Oct 7 doi: 10.1016/j.bone.2016.10.004. PMID: 27725317
Oshima M, Tsuji T
Adv Exp Med Biol 2015;881:255-69. doi: 10.1007/978-3-319-22345-2_14. PMID: 26545754

Recent clinical studies

Etiology

Danze A, Jacox LA, Bocklage C, Whitley J, Moss K, Hardigan P, Garcia-Godoy CE, Jackson TH
Eur J Orthod 2021 Apr 3;43(2):184-192. doi: 10.1093/ejo/cjaa056. PMID: 32968775
Yang S, Jung BY, Pang NS
Clin Oral Investig 2019 Jan;23(1):87-98. Epub 2018 Mar 10 doi: 10.1007/s00784-018-2412-3. PMID: 29525925
Frazier-Bowers S, Zanardi G, Mendes Miguel JA, Almeida R, Machado Cruz R
Dental Press J Orthod 2015 Mar-Apr;20(2):22-8. doi: 10.1590/2176-9451.20.2.022-028.int. PMID: 25992983Free PMC Article
Blechman AM
Am J Orthod Dentofacial Orthop 1998 Apr;113(4):379-83. PMID: 9563351
Pirinen S
Acta Odontol Scand 1995 Jun;53(3):179-85. doi: 10.3109/00016359509005969. PMID: 7572094

Diagnosis

Muthu MS, Vandana S, Akila G, Anusha M, Kandaswamy D, Aswath Narayanan MB
Arch Oral Biol 2024 Feb;158:105857. Epub 2023 Dec 6 doi: 10.1016/j.archoralbio.2023.105857. PMID: 38128337
Goldstein G, Goodacre C, MacGregor K
J Prosthodont 2021 Apr;30(S1):12-19. doi: 10.1111/jopr.13315. PMID: 33783090
Akkuc S, Duruk G, Duman S
Oral Radiol 2021 Jul;37(3):476-486. Epub 2020 Sep 19 doi: 10.1007/s11282-020-00482-7. PMID: 32949336
Ong DV, Dance GM
Aust Dent J 2021 Mar;66(1):85-95. Epub 2020 May 10 doi: 10.1111/adj.12757. PMID: 32278321
Garcovich D, Aiuto R, Lozano Serrano E, Re D
Eur J Paediatr Dent 2018 Dec;19(4):300-302. doi: 10.23804/ejpd.2018.19.04.9. PMID: 30567447

Therapy

Vandana S, Muthu MS, Akila G, Anusha M, Kandaswamy D, Aswath Narayanan MB
Am J Hum Biol 2024 Aug;36(8):e24060. Epub 2024 Mar 1 doi: 10.1002/ajhb.24060. PMID: 38426348
Goldstein G, Goodacre C, MacGregor K
J Prosthodont 2021 Apr;30(S1):12-19. doi: 10.1111/jopr.13315. PMID: 33783090
Paglia L
Eur J Paediatr Dent 2016 Sep;17(3):173. PMID: 27759403
Feigal RJ
Pediatr Dent 1998 Mar-Apr;20(2):85-92. PMID: 9566011
Blechman AM
Am J Orthod Dentofacial Orthop 1998 Apr;113(4):379-83. PMID: 9563351

Prognosis

Kim J, Jung S, Lee KJ, Yu HS, Park W
BMC Oral Health 2024 Feb 20;24(1):254. doi: 10.1186/s12903-024-03963-x. PMID: 38378499Free PMC Article
Ong DV, Dance GM
Aust Dent J 2021 Mar;66(1):85-95. Epub 2020 May 10 doi: 10.1111/adj.12757. PMID: 32278321
Yang S, Jung BY, Pang NS
Clin Oral Investig 2019 Jan;23(1):87-98. Epub 2018 Mar 10 doi: 10.1007/s00784-018-2412-3. PMID: 29525925
Frazier-Bowers S, Zanardi G, Mendes Miguel JA, Almeida R, Machado Cruz R
Dental Press J Orthod 2015 Mar-Apr;20(2):22-8. doi: 10.1590/2176-9451.20.2.022-028.int. PMID: 25992983Free PMC Article
Feigal RJ
Pediatr Dent 1998 Mar-Apr;20(2):85-92. PMID: 9566011

Clinical prediction guides

Kim J, Jung S, Lee KJ, Yu HS, Park W
BMC Oral Health 2024 Feb 20;24(1):254. doi: 10.1186/s12903-024-03963-x. PMID: 38378499Free PMC Article
Garib D, Miranda F, Massaro C, Lauris JRP, Yatabe MS, Janson G, McNamara JA Jr, Behrents RG, Cevidanes LHS, Ruellas ACO
Am J Orthod Dentofacial Orthop 2021 Feb;159(2):184-192. Epub 2020 Dec 31 doi: 10.1016/j.ajodo.2019.12.021. PMID: 33388202Free PMC Article
Ong DV, Dance GM
Aust Dent J 2021 Mar;66(1):85-95. Epub 2020 May 10 doi: 10.1111/adj.12757. PMID: 32278321
Yang S, Jung BY, Pang NS
Clin Oral Investig 2019 Jan;23(1):87-98. Epub 2018 Mar 10 doi: 10.1007/s00784-018-2412-3. PMID: 29525925
de Lima EM, Schmidt CB, de Araujo LL, Rizzatto SM, Martinelli FL
Angle Orthod 2012 Nov;82(6):1067-70. Epub 2012 Apr 4 doi: 10.2319/092111-600.1. PMID: 22475327Free PMC Article

Recent systematic reviews

Vandana S, Muthu MS, Akila G, Anusha M, Kandaswamy D, Aswath Narayanan MB
Am J Hum Biol 2024 Aug;36(8):e24060. Epub 2024 Mar 1 doi: 10.1002/ajhb.24060. PMID: 38426348
Muthu MS, Vandana S, Akila G, Anusha M, Kandaswamy D, Aswath Narayanan MB
Arch Oral Biol 2024 Feb;158:105857. Epub 2023 Dec 6 doi: 10.1016/j.archoralbio.2023.105857. PMID: 38128337
Aravena-Salazar JP, Matus-Miranda G, Dethlefs-Canto J, Niklander SE
Med Oral Patol Oral Cir Bucal 2024 Mar 1;29(2):e241-e247. doi: 10.4317/medoral.26233. PMID: 37823295Free PMC Article
Araujo VZ, Heckmann S, Araujo FB, Casagrande L, Ziegelmann PK, Araújo EA, Marques LS, Lenzi TL
Braz Oral Res 2023;36:e119. Epub 2023 Jan 16 doi: 10.1590/1807-3107bor-2022.vol36.0119. PMID: 36651386
Furquim CP, Kumagai RY, Bustillos-Torrez W, Meza-Mauricio J, Tanaka CJ, Santana V, Retamal-Valdes B, Shibli JA
Tissue Eng Part C Methods 2022 Mar;28(3):104-112. doi: 10.1089/ten.TEC.2022.0022. PMID: 35172636

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