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30 Possible Causes for Congenital Facial Anomaly, correa, Gingival Recession

Did you mean: Congenital Facial Anomaly, cornea, Gingival Recession

  • Bruxism

    Júnia Maria Serra-Negra, Frank Lobbezoo, Patricia Correa-Faria, Luca Lombardo, Giuseppe Siciliani, Edoardo Stellini and Daniele Manfredini, Relationship of self-reported sleep[doi.org] recession, tooth mobility, fractured restorations, masticatory muscle pain, and temporomandibular disorders.[emedicine.medscape.com] FH van de Sande, K Collares, MB Correa, MS Cenci, FF Demarco and NJM Opdam, Restoration Survival: Revisiting Patients' Risk Factors Through a Systematic Literature Review,[doi.org]

  • Dental Caries

    Macias M, Bustamante ZM, Camargo L, Correa P, Hernández ME. Estado de salud bucal en preescolares de nivel socioeconómico alto y medio alto. [Thesis].[scielo.br] Root caries develops only when gingival recession exposes cementum through periodontal disease, a feature of advancing age in many animals.[carta.anthropogeny.org] PubMed View Article Google Scholar Vieira-Andrade RG, Martins-Junior PA, Correa-Faria P, Stella PE, Marinho SA, Marques LS, et al.[bmcoralhealth.biomedcentral.com]

  • Ameloblastoma

    Leonardo Nogueira Rodrigues, GefterThiago Batista Correa, Marina Gonçalves Diniz, Clarice Ferreira Galvão, Carolina Cavaliéri Gomes and Ricardo Santiago Gomez, BRAF V600E[doi.org] The goal is to prevent later gingival recession as well as the unaesthetic appearance of an implant shining through a thin gingiva. more » Watch free preview Watch free preview[dental-online-college.com] […] of chronic periodontitis -- Gingival recession -- Aggressive periodontitis -- Prepubertal' periodontitis -- Periodontitis as a manifestation of systemic disease -- Down's[worldcat.org]

  • Seckel Syndrome

    Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, Correa A (2010).[centogene.com] She presented with interesting dental findings, including gingival hyperplasia, recession and ulceration, significant crowding, and early exfoliation of the primary dentition[ncbi.nlm.nih.gov]

  • Congenital Mandibular Hypoplasia

    Hemifacial microsomia ( HFM ) is the second most common congenital facial anomaly after cleft lip/palate. The condition may vary from mild to severe.[radiopaedia.org] […] infrazygomatic SMAS P Morales 167 the argon gas surgical unit D Man and H Plosker 173 Improving mammaplasty scars with lipoplasty E B de Souza Pinto P J Erazo I A C Muniz and J P T Correa[books.google.com] The intraoral examination revealed Angle Class II malocclusion and an overjet of 4.5 mm, horizontal bone loss and gingival recession in the maxilla and mandible (Figure 2)[medical-case-reports.imedpub.com]

  • Hereditary Gingival Fibromatosis

    […] and cerebellar anomalies, mild mental retardation, mixed hearing loss and facial dysmorphism.[nature.com] Chronic periodontitis Epidemiology of periodontal diseases Gingivitis Gum graft Periodontist Tooth loss Gingival recession American Academy of Periodontology Home Page Periodontal[en.wikipedia.org] Winters, “Hereditary gingival fibromatosis with a recessive mode of inheritance. Case reports,” Australian Dental Journal, vol. 38, no. 6, pp. 427–432, 1993.[ipfs.io]

  • Gingival Fibromatosis-Progressive Deafness Syndrome

    […] and cerebellar anomalies, mild mental retardation, mixed hearing loss and facial dysmorphism.[nature.com] Autosomal recessive gingival fibromatosis with distinctive facies.[documentslide.com] Clin Genet 1992;42:306-8.Holzhausen M, Goncalves D, Correa Fde O, Spolidorio LC,Rodrigues VC, Orrico SR. A case of Zimmermann-Laband syn-drome with supernumerary teeth.[docslide.com.br]

  • Knobloch Syndrome Type 1

    HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER Congenital Hydronephrosis, with Cleft Palate, Characteristic Facies, Hypotonia, and Mental[rgd.mcw.edu] Armelin-Correa, Andréa L. Sertié, Flavia I.V. Errera, Kelly Bagatini, Fernando Kok and Katia R.M.[dx.doi.org] Hereditary gingival fibromatosis  both dominant autosomal inheritance and recessive autosomal inheritance  It is a gradually progressive benign enlargement that affects[slideshare.net]

  • Wiedemann-Steiner Syndrome

    Wiedemann-Steiner syndrome (WSS) is an autosomal dominant congenital anomaly syndrome characterized by hairy elbows, dysmorphic facial appearances (hypertelorism, thick eyebrows[ncbi.nlm.nih.gov] Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, Correa A (2010).[centogene.com] References (Supplied by CrossRef) A distinct osteochondrodysplasia with hypertrichosis-Individualization of a probable autosomal recessive entity Cantu et al.[pubfacts.com]

  • Familial Median Cleft of the Upper and Lower Lips

    A cleft palate is a common congenital facial anomaly treated by plastic surgeons.[verywell.com] Correa A, Gilboa SM, Besser LM, et al; National Birth Defects Prevention Study. Diabetes mellitus and birth defects. Am J Obstet Gynecol. 2008;199(3):237.e1-237.e9. 13.[consultant360.com] recession in relation to 16,17, 26, 27, 31, 32, 33, 36, 37, 41, 42, 43, 46, and 47.[jiaomr.in]