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Abnormal oral physiology

MedGen UID:
1631824
•Concept ID:
C4703551
•
Disease or Syndrome
HPO: HP:0031815

Definition

A functional anomaly of the mouth (which is also known as the oral cavity). [from HPO]

Professional guidelines

PubMed

Diagnosis and Management of Multiple Myeloma: A Review.
Cowan AJ, Green DJ, Kwok M, Lee S, Coffey DG, Holmberg LA, Tuazon S, Gopal AK, Libby EN
JAMA 2022 Feb 1;327(5):464-477. doi: 10.1001/jama.2022.0003. PMID: 35103762
Clinical Management of Hyperkalemia.
Palmer BF, Carrero JJ, Clegg DJ, Colbert GB, Emmett M, Fishbane S, Hain DJ, Lerma E, Onuigbo M, Rastogi A, Roger SD, Spinowitz BS, Weir MR
Mayo Clin Proc 2021 Mar;96(3):744-762. Epub 2020 Nov 5 doi: 10.1016/j.mayocp.2020.06.014. PMID: 33160639
Diagnosis and treatment of temporomandibular disorders.
Gauer RL, Semidey MJ
Am Fam Physician 2015 Mar 15;91(6):378-86. PMID: 25822556

Recent clinical studies

Etiology

Hypophosphatasia: oral cavity and dental disorders.
Bloch-Zupan A, Vaysse F
Arch Pediatr 2017 May;24(5S2):5S80-5S84. doi: 10.1016/S0929-693X(18)30020-4. PMID: 29405938
On the Etiology of Molar-Incisor Hypomineralization.
Vieira AR, Kup E
Caries Res 2016;50(2):166-9. Epub 2016 Apr 26 doi: 10.1159/000445128. PMID: 27111773
Meier-Gorlin syndrome.
de Munnik SA, Hoefsloot EH, Roukema J, Schoots J, Knoers NV, Brunner HG, Jackson AP, Bongers EM
Orphanet J Rare Dis 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x. PMID: 26381604Free PMC Article
Preterm infants--odontological aspects.
Rythén M
Swed Dent J Suppl 2012;(224):2p preceding i-vi, 1-106. PMID: 22755470
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
Barron MJ, McDonnell ST, Mackie I, Dixon MJ
Orphanet J Rare Dis 2008 Nov 20;3:31. doi: 10.1186/1750-1172-3-31. PMID: 19021896Free PMC Article

Diagnosis

Meier-Gorlin syndrome.
de Munnik SA, Hoefsloot EH, Roukema J, Schoots J, Knoers NV, Brunner HG, Jackson AP, Bongers EM
Orphanet J Rare Dis 2015 Sep 17;10:114. doi: 10.1186/s13023-015-0322-x. PMID: 26381604Free PMC Article
Anatomy and physiology of velopharyngeal closure and insufficiency.
Raol N, Hartnick CJ
Adv Otorhinolaryngol 2015;76:1-6. Epub 2015 Feb 19 doi: 10.1159/000368003. PMID: 25733226
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
Barron MJ, McDonnell ST, Mackie I, Dixon MJ
Orphanet J Rare Dis 2008 Nov 20;3:31. doi: 10.1186/1750-1172-3-31. PMID: 19021896Free PMC Article
KBG syndrome.
Brancati F, Sarkozy A, Dallapiccola B
Orphanet J Rare Dis 2006 Dec 12;1:50. doi: 10.1186/1750-1172-1-50. PMID: 17163996Free PMC Article
Tongue-tie.
Catlin FI
Arch Otolaryngol 1971 Dec;94(6):548-57. doi: 10.1001/archotol.1971.00770070848010. PMID: 4942948

Therapy

Gene-environment interaction in molar-incisor hypomineralization.
Bezamat M, Souza JF, Silva FMF, Corrêa EG, Fatturi AL, Brancher JA, Carvalho FM, Cavallari T, Bertolazo L, Machado-Souza C, Koruyucu M, Bayram M, Racic A, Harrison BM, Sweat YY, Letra A, Studen-Pavlovich D, Seymen F, Amendt B, Werneck RI, Costa MC, Modesto A, Vieira AR
PLoS One 2021;16(1):e0241898. Epub 2021 Jan 6 doi: 10.1371/journal.pone.0241898. PMID: 33406080Free PMC Article
Protein-mediated enamel mineralization.
Moradian-Oldak J
Front Biosci (Landmark Ed) 2012 Jun 1;17(6):1996-2023. doi: 10.2741/4034. PMID: 22652761Free PMC Article
Food safety.
Borchers A, Teuber SS, Keen CL, Gershwin ME
Clin Rev Allergy Immunol 2010 Oct;39(2):95-141. doi: 10.1007/s12016-009-8176-4. PMID: 19911313
Heart diseases and stroke.
Sila CA
Curr Neurol Neurosci Rep 2006 Jan;6(1):23-7. doi: 10.1007/s11910-996-0005-z. PMID: 16469267
Amenorrhea.
Marchant DJ
Clin Obstet Gynecol 1969 Sep;12(3):693-707. doi: 10.1097/00003081-196909000-00010. PMID: 5388335

Prognosis

Abnormal cytology in oropharyngeal brushings and in oral rinses is not associated with HPV infection: The OHMAR study.
Benevolo M, Rollo F, Giuliani M, Pichi B, Latini A, Pellini R, Vescio MF, Morrone A, Cristaudo A, Donà MG
Cancer Cytopathol 2020 Sep;128(9):648-655. Epub 2020 Jun 2 doi: 10.1002/cncy.22295. PMID: 32485093
Congenital diseases of the gastrointestinal tract.
Lentze M
Georgian Med News 2014 May;(230):46-53. PMID: 24940857
Clinical and molecular features of Joubert syndrome and related disorders.
Parisi MA
Am J Med Genet C Semin Med Genet 2009 Nov 15;151C(4):326-40. doi: 10.1002/ajmg.c.30229. PMID: 19876931Free PMC Article
Costello syndrome: an overview.
Hennekam RC
Am J Med Genet C Semin Med Genet 2003 Feb 15;117C(1):42-8. doi: 10.1002/ajmg.c.10019. PMID: 12561057
Down's syndrome and oral care.
Fiske J, Shafik HH
Dent Update 2001 Apr;28(3):148-56. doi: 10.12968/denu.2001.28.3.148. PMID: 11819976

Clinical prediction guides

Developmental Defects of Enamel.
Martins DDS, Ionta FQ, Pompermaier Garlet G, Lima RR, Neves AA, Rios D, Lussi A
Monogr Oral Sci 2024;32:10-34. Epub 2024 Jul 1 doi: 10.1159/000538850. PMID: 39321764
Hypodontia: An Update on Its Etiology, Classification, and Clinical Management.
Al-Ani AH, Antoun JS, Thomson WM, Merriman TR, Farella M
Biomed Res Int 2017;2017:9378325. Epub 2017 Mar 19 doi: 10.1155/2017/9378325. PMID: 28401166Free PMC Article
KBG syndrome.
Brancati F, Sarkozy A, Dallapiccola B
Orphanet J Rare Dis 2006 Dec 12;1:50. doi: 10.1186/1750-1172-1-50. PMID: 17163996Free PMC Article
Further delineation of the branchio-oculo-facial syndrome.
Lin AE, Gorlin RJ, Lurie IW, Brunner HG, van der Burgt I, Naumchik IV, Rumyantseva NV, Stengel-Rutkowski S, Rosenbaum K, Meinecke P
Am J Med Genet 1995 Mar 13;56(1):42-59. doi: 10.1002/ajmg.1320560112. PMID: 7747785
Oral-pharyngeal development and evaluation.
Ogg HL
Phys Ther 1975 Mar;55(3):235-41. doi: 10.1093/ptj/55.3.235. PMID: 1089974

Recent systematic reviews

Gastroschisis: a systematic review of diagnosis, prognosis and treatment.
Ferreira RG, Mendonça CR, Gonçalves Ramos LL, de Abreu Tacon FS, Naves do Amaral W, Ruano R
J Matern Fetal Neonatal Med 2022 Dec;35(25):6199-6212. Epub 2021 Apr 25 doi: 10.1080/14767058.2021.1909563. PMID: 33899664
Advances in Pathogenesis of Sjögren's Syndrome.
Tian Y, Yang H, Liu N, Li Y, Chen J
J Immunol Res 2021;2021:5928232. Epub 2021 Oct 7 doi: 10.1155/2021/5928232. PMID: 34660815Free PMC Article
Down syndrome as a cause of abnormalities in the craniofacial region: A systematic literature review.
Kaczorowska N, Kaczorowski K, Laskowska J, Mikulewicz M
Adv Clin Exp Med 2019 Nov;28(11):1587-1592. doi: 10.17219/acem/112785. PMID: 31778604
Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women.
Carmina E, Dewailly D, Escobar-Morreale HF, Kelestimur F, Moran C, Oberfield S, Witchel SF, Azziz R
Hum Reprod Update 2017 Sep 1;23(5):580-599. doi: 10.1093/humupd/dmx014. PMID: 28582566
Oral Spironolactone for Acne Vulgaris in Adult Females: A Hybrid Systematic Review.
Layton AM, Eady EA, Whitehouse H, Del Rosso JQ, Fedorowicz Z, van Zuuren EJ
Am J Clin Dermatol 2017 Apr;18(2):169-191. doi: 10.1007/s40257-016-0245-x. PMID: 28155090Free PMC Article

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