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Tooth disorder

MedGen UID:
11852
•Concept ID:
C0040435
•
Disease or Syndrome
Synonym: Tooth disease
SNOMED CT: Tooth disease (234947003); Tooth disorder (234947003)
 
Monarch Initiative: MONDO:0006999

Definition

A disease involving the calcareous tooth. [from MONDO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVTooth disorder

Professional guidelines

PubMed

Prevention and treatment of peri-implant diseases-The EFP S3 level clinical practice guideline.
Herrera D, Berglundh T, Schwarz F, Chapple I, Jepsen S, Sculean A, Kebschull M, Papapanou PN, Tonetti MS, Sanz M; EFP workshop participants and methodological consultant
J Clin Periodontol 2023 Jun;50 Suppl 26:4-76. Epub 2023 Jun 4 doi: 10.1111/jcpe.13823. PMID: 37271498
Treatment of stage IV periodontitis: The EFP S3 level clinical practice guideline.
Herrera D, Sanz M, Kebschull M, Jepsen S, Sculean A, Berglundh T, Papapanou PN, Chapple I, Tonetti MS; EFP Workshop Participants and Methodological Consultant
J Clin Periodontol 2022 Jun;49 Suppl 24:4-71. doi: 10.1111/jcpe.13639. PMID: 35688447
European Society of Endodontology position statement: Management of deep caries and the exposed pulp.
European Society of Endodontology (ESE) developed by:, Duncan HF, Galler KM, Tomson PL, Simon S, El-Karim I, Kundzina R, Krastl G, Dammaschke T, Fransson H, Markvart M, Zehnder M, Bjørndal L
Int Endod J 2019 Jul;52(7):923-934. doi: 10.1111/iej.13080. PMID: 30664240

Recent clinical studies

Etiology

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
Chow CY, Zhang Y, Dowling JJ, Jin N, Adamska M, Shiga K, Szigeti K, Shy ME, Li J, Zhang X, Lupski JR, Weisman LS, Meisler MH
Nature 2007 Jul 5;448(7149):68-72. Epub 2007 Jun 17 doi: 10.1038/nature05876. PMID: 17572665Free PMC Article
Nuclear matrix proteins and hereditary diseases.
Sjakste N, Sjakste T
Genetika 2005 Mar;41(3):293-8. PMID: 15865282
Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse.
De Sandre-Giovannoli A, Chaouch M, Kozlov S, Vallat JM, Tazir M, Kassouri N, Szepetowski P, Hammadouche T, Vandenberghe A, Stewart CL, Grid D, Lévy N
Am J Hum Genet 2002 Mar;70(3):726-36. Epub 2002 Jan 17 doi: 10.1086/339274. PMID: 11799477Free PMC Article
CPITN, DMFT, and treatment requirements in a Nicaraguan population.
Smith AC, Lang WP
Community Dent Oral Epidemiol 1993 Aug;21(4):190-3. doi: 10.1111/j.1600-0528.1993.tb00754.x. PMID: 8370253
Neurophysiological aspects of peripheral neuropathies.
MacKenzie RA, Skuse NF, Lethlean AK
Proc Aust Assoc Neurol 1976;13:43-9. PMID: 196281

Diagnosis

Endodontic Treatment of Hypertaurodontic Mandibular Molar Using Reciprocating Single-file System: A Case Report.
C do Nascimento A, A F Marques A, C Sponchiado-Júnior E, F R Garcia L, M A de Carvalho F
Bull Tokyo Dent Coll 2016;57(2):83-9. doi: 10.2209/tdcpublication.2015-0033. PMID: 27320297

Therapy

CPITN, DMFT, and treatment requirements in a Nicaraguan population.
Smith AC, Lang WP
Community Dent Oral Epidemiol 1993 Aug;21(4):190-3. doi: 10.1111/j.1600-0528.1993.tb00754.x. PMID: 8370253

Prognosis

An In Vitro Model of Charcot-Marie-Tooth Disease Type 4B2 Provides Insight Into the Roles of MTMR13 and MTMR2 in Schwann Cell Myelination.
Robinson DC, Mammel AE, Logan AM, Larson AA, Schmidt EJ, Condon AF, Robinson FL
ASN Neuro 2018 Jan-Dec;10:1759091418803282. doi: 10.1177/1759091418803282. PMID: 30419760Free PMC Article

Clinical prediction guides

An In Vitro Model of Charcot-Marie-Tooth Disease Type 4B2 Provides Insight Into the Roles of MTMR13 and MTMR2 in Schwann Cell Myelination.
Robinson DC, Mammel AE, Logan AM, Larson AA, Schmidt EJ, Condon AF, Robinson FL
ASN Neuro 2018 Jan-Dec;10:1759091418803282. doi: 10.1177/1759091418803282. PMID: 30419760Free PMC Article
Connexin 32 is involved in mitosis.
Mones S, Bordignon B, Fontes M
Glia 2012 Mar;60(3):457-64. Epub 2011 Nov 30 doi: 10.1002/glia.22279. PMID: 22131286
Dominant Intermediate Charcot-Marie-Tooth disorder is not due to a catalytic defect in tyrosyl-tRNA synthetase.
Froelich CA, First EA
Biochemistry 2011 Aug 23;50(33):7132-45. Epub 2011 Jul 26 doi: 10.1021/bi200989h. PMID: 21732632
Amelogenin signal peptide mutation: correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta.
Lagerström-Fermér M, Nilsson M, Bäckman B, Salido E, Shapiro L, Pettersson U, Landegren U
Genomics 1995 Mar 1;26(1):159-62. doi: 10.1016/0888-7543(95)80097-6. PMID: 7782077

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