Association of Taurodontism with Hypodontia: a Controlled Study W
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Glossary for Narrative Writing
Periodontal Assessment and Treatment Planning Gingival description Color: o pink o erythematous o cyanotic o racial pigmentation o metallic pigmentation o uniformity Contour: o recession o clefts o enlarged papillae o cratered papillae o blunted papillae o highly rolled o bulbous o knife-edged o scalloped o stippled Consistency: o firm o edematous o hyperplastic o fibrotic Band of gingiva: o amount o quality o location o treatability Bleeding tendency: o sulcus base, lining o gingival margins Suppuration Sinus tract formation Pocket depths Pseudopockets Frena Pain Other pathology Dental Description Defective restorations: o overhangs o open contacts o poor contours Fractured cusps 1 ww.links2success.biz [email protected] 914-303-6464 Caries Deposits: o Type . plaque . calculus . stain . matera alba o Location . supragingival . subgingival o Severity . mild . moderate . severe Wear facets Percussion sensitivity Tooth vitality Attrition, erosion, abrasion Occlusal plane level Occlusion findings Furcations Mobility Fremitus Radiographic findings Film dates Crown:root ratio Amount of bone loss o horizontal; vertical o localized; generalized Root length and shape Overhangs Bulbous crowns Fenestrations Dehiscences Tooth resorption Retained root tips Impacted teeth Root proximities Tilted teeth Radiolucencies/opacities Etiologic factors Local: o plaque o calculus o overhangs 2 ww.links2success.biz [email protected] 914-303-6464 o orthodontic apparatus o open margins o open contacts o improper -
Oral Health in Prevalent Types of Ehlers–Danlos Syndromes
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Ghent University Academic Bibliography J Oral Pathol Med (2005) 34: 298–307 ª Blackwell Munksgaard 2005 Æ All rights reserved www.blackwellmunksgaard.com/jopm Oral health in prevalent types of Ehlers–Danlos syndromes Peter J. De Coster1, Luc C. Martens1, Anne De Paepe2 1Department of Paediatric Dentistry, Centre for Special Care, Paecamed Research, Ghent University, Ghent; 2Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium BACKGROUND: The Ehlers–Danlos syndromes (EDS) Introduction comprise a heterogenous group of heritable disorders of connective tissue, characterized by joint hypermobility, The Ehlers–Danlos syndromes (EDS) comprise a het- skin hyperextensibility and tissue fragility. Most EDS erogenous group of heritable disorders of connective types are caused by mutations in genes encoding different tissue, largely characterized by joint hypermobility, skin types of collagen or enzymes, essential for normal pro- hyperextensibility and tissue fragility (1) (Fig. 1). The cessing of collagen. clinical features, modes of inheritance and molecular METHODS: Oral health was assessed in 31 subjects with bases differ according to the type. EDS are caused by a EDS (16 with hypermobility EDS, nine with classical EDS genetic defect causing an error in the synthesis or and six with vascular EDS), including signs and symptoms processing of collagen types I, III or V. The distribution of temporomandibular disorders (TMD), alterations of and function of these collagen types are displayed in dental hard tissues, oral mucosa and periodontium, and Table 1. At present, two classifications of EDS are was compared with matched controls. -
Oral and Craniofacial Manifestations of Ellis-Van Creveld Syndrome Were Pointed Manifestations, Since the Dentist May Be the First Clinician Out
Oral and craniofacial manifestations D. Lauritano, S. Attuati, M. Besana, G. Rodilosso, V. Quinzi*, G. Marzo*, of Ellis-Van Creveld F. Carinci** Department of medicine and surgery, Neuroscience Centre of Milan, University of Milan-Bicocca, Milan, Italy. syndrome: a systematic *Post Graduate School of Orthodontic, Department of Life, Health and Environmental Sciences, University of L´Aquila, Italy **Department of Morphology, Surgery and Experimental review Medicine, University of Ferrara, Ferrara, Italy e-mail: [email protected] DOI 10.23804/ejpd.2019.20.04.09 Abstract their patients. The typical clinical manifestations include chondrodysplasia, ectodermal dysplasia (dystrophic nails, hypodontia and malformed teeth), polydactyly and congenital Aim A systematic literature review on oral and craniofacial heart disease. Cognitive development is usually normal. manifestations of Ellis-Van Creveld syndrome was performed. Dental anomalies consist of peg-shaped teeth, prenatal Methods From 2 databases were selected 74 articles using as key words “Ellis-Van Creveld” AND “Oral” OR “Craniofacial” teeth or delayed eruption, hypodontia, taurodontism, micro- OR “Dental” OR “Malocclusion”. Prisma protocol was used to or macrodontia and enamel hypoplasia, which may affect create an eligible list for the screening. Data were collected in a nutrition of these patients. table to compare the clinical aspects found. A delay in diagnosis is due to the lack of proper screening. Results From the first research emerged 350 articles, and only 72 of them were selected. Objectives Conclusion Through this analysis oral and cranio-facial The aim of this study is to point out oral and craniofacial manifestations of Ellis-Van Creveld syndrome were pointed manifestations, since the dentist may be the first clinician out. -
Dental Management of the Head and Neck Cancer Patient Treated
Dental Management of the Head and Neck Cancer Patient Treated with Radiation Therapy By Carol Anne Murdoch-Kinch, D.D.S., Ph.D., and Samuel Zwetchkenbaum, D.D.S., M.P.H. pproximately 36,540 new cases of oral cavity and from radiation injury to the salivary glands, oral mucosa pharyngeal cancer will be diagnosed in the USA and taste buds, oral musculature, alveolar bone, and this year; more than 7,880 people will die of this skin. They are clinically manifested by xerostomia, oral A 1 disease. The vast majority of these cancers are squamous mucositis, dental caries, accelerated periodontal disease, cell carcinomas. Most cases are diagnosed at an advanced taste loss, oral infection, trismus, and radiation dermati- stage: 62 percent have regional or distant spread at the tis.4 Some of these effects are acute and reversible (muco- time of diagnosis.2 The five-year survival for all stages sitis, taste loss, oral infections and xerostomia) while oth- combined is 61 percent.1 Localized tumors (Stage I and II) ers are chronic (xerostomia, dental caries, accelerated can usually be treated surgically, but advanced cancers periodontal disease, trismus, and osteoradionecrosis.) (Stage III and IV) require radiation with or without che- Chemotherapeutic agents may be administered as an ad- motherapy as adjunctive or definitive treatment.1 See Ta- junct to RT. Patients treated with multimodality chemo- ble 1.3 Therefore, most patients with oral cavity and pha- therapy and RT may be at greater risk for oral mucositis ryngeal cancer receive head and neck radiation therapy and secondary oral infections such as candidiasis. -
Feline Health Topics for Veterinarians
Feline Health Topics for veterinarians Volume 6 , Number 4 Feline Oral and Dental Diseases John E. Saidla, D.V.M. Although oral and dental diseases occur frequently The maxillary PM’s are PM2, PM3 and PM4, in the cat, they are often overlooked. Performing an while the mandibular are PM3 and PM4. The decidu oral examination on a cat can be problematic, partially ous incisors and canine teeth of the cat erupt between due to the relatively tight lips that surround the cat’ s 3 to 4 weeks and the premolars between 5 to 6 weeks. small oral cavity. Also, many of the common dental The incisors are replaced between 3 1/2 and 5 1/2 and oral problems cause significant pain, making months, the canines between 5 1/2 and 61/2 months, cats even less tolerant of the examination. Therefore, the premolars between 4 to 5 months, and the molars anesthesia or sedation is usually required to perform between 5 to 6 months. a thorough oral examination and radiography of the Permanent Dentition: cat’ s mouth. (13/3, C l/1 , PM 3/2, M l/1 ) x 2 = 30 teeth Anatomy The camassial teeth are maxillary PM4 and man Knowing the dental anatomy and formulas are espe dibular M l. The premolars are designated the same cially important since cats have fewer teeth as numbers as in the deciduous dentition.7 There is one compared to other mammals. Knowing which teeth root for each incisor and canine tooth, the maxillary are anatomically missing improves the probability PM3 has two roots, PM4 has three roots, M l has two that one can identify truly missing teeth. -
Ovarian Cancer
113th AAO Annual Session OVERVIEW Unraveling an Association between Hypodontia and OUTLINE Epithelial Ovarian Cancer 1. Introduction Anna N Vu, DMD, MS 2. Background 3. Purpose Division of Orthodontics 4. Materials and Methods May 2013 5. Results 6. Discussion 7. Conclusion U N I V E R S I T Y O F K E N T U C K Y C O L L E G E O F D E N T I S T R Y HYPODONTIA HYPODONTIA REVIEW & CANCER • Over 300 genes are involved in odontogenesis including MSX1, PAX9, and AXIN2 HYPODONTIA • Genes involved in dental development also have roles in other organs of the body Defined as the developmental absence of one or more teeth as well as variations in size, • Mutation in several genes governing tooth development have already been associated with shape, rate of dental development and eruption time. cancer • Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer7 Hypodontia is the agenesis of 6 or less teeth. • AXIN2 gene is highly expressed in ovarian tissue so may play a role in epithelial ovarian cancer (EOC)8 Oligodontia is the agenesis of 6 or more teeth. Anodontia is the agenesis of all teeth. • Reduced expression of PAX9 can lead to hypodontia and has been correlated with increased malignancy of dysplastic and cancerous esophageal epithelium9 2.6-11.3% reported prevelance worldwide. 78 • RUNX transcription factor family (RUNX1, 2, and 3) are involved in odontogenesis and has been Women are affected more than males at a ratio of 3:2. the most targeted genes in acute myeloid leukemia and acute lymphoblastic leukemia10 Both genetic and environmental explanations for hypodontia have been reported. -
Current Approaches for Tooth Agenesis: a Review
Atatürk Üniv. Diş Hek. Fak. Derg. Derleme/ ŞENTÜRK, Review ULU GÜZEL J Dent Fac Atatürk Uni Cilt:29, Sayı:2, Yıl: 2019, Sayfa, 332-339 CURRENT APPROACHES FOR TOOTH AGENESIS: A REVIEW DIŞ EKSIKLIĞINDE GÜNCEL YAKLAŞIMLAR: DERLEME Arş. Gör. Dt. Özge ŞENTÜRK* Dr. Öğr. Üyesi Kadriye Görkem ULU GÜZEL* Makale Kodu/Article code: 3126 Makale Gönderilme tarihi: 10.11.2016 Kabul Tarihi: 29.12.2016 ABSTRACT ÖZ Hypodontia is defined as the congenital deficiency of one or more teeth and is one of the most common Hipodonti, bir veya daha fazla dişin konjenital eksikliği dental anomalies in humans. Multifactorial etiology can olarak tanımlanır ve insanlarda en sık görülen dental include environmental factors as well, since a anomalilerden biridir. Genetik faktörlerin yanısıra combination of environmental and genetic factors çevresel faktörler veya bunların kombinasyonu diş might contribute to the occurrence of dental agenesis. eksikliklerinin görülmesine sebep olabilmektedir. Eksik Patient with missing teeth; reduced masticatory dişlere sahip hastalar; azalmış çiğneme yeteneği, ability, inarticulate pronunciation may encounter telaffuzun anlaşılamaması, estetik ve periodontal esthetics and periodontal problems. Tooth agenesis problemlerle karşılaşabilmektedir. Bu derlemede definition, etiology, genes that cause tooth agenesis konjenital diş eksikliği tanımı, etiyolojisi, diş eksikliğine and treatment of tooth agenesis is mentioned in this sebep olan genler ve tedavisinden bahsedilmektedir. review. Nowadays, many genes which play role in Günümüzde, diş -
Taurodontism –A Review on Its Etiology, Prevalence and Clinical Considerations
J Clin Exp Dent. 2010;2(4):e187-90. Taurodontism –A Review on its etiology. Journal section: Oral Medicine and Pathology doi:10.4317/jced.2.e187 Publication Types: Review Taurodontism –A Review on its etiology, prevalence and clinical considerations BS Manjunatha 1, Suresh Kumar Kovvuru 2 1 BDS, MDS, (DNB), FAGE, Reader in Oral and Maxillofacial Pathology. Sumandeep Vidyapeeth. K M Shah Dental College & Hospital, Pipariya, 391760, Waghodia (T), Vadodara (D). Gujarat State, INDIA. 2 BDS, MDS, Assistant Professor. Department of Conservative Dentistry & Endodontics. Sumandeep Vidyapeeth. K M Shah Dental College & Hospital, Pipariya, 391760, Waghodia (T), Vadodara (D). Gujarat State, INDIA. Correspondence: K M Shah Dental College & Hospital, Pipariya—391760, Waghodia (T), Vadodara (D) Gujarat State, INDIA. E- mail: [email protected] Manjunatha BS, Kovvuru SK. Taurodontism –A Review on its etiology, prevalence and clinical considerations. J Clin Exp Dent. 2010;2(4):e187- Received: 30/07/2010 Accepted: 06/09/2010 90. http://www.medicinaoral.com/odo/volumenes/v2i4/jcedv2i4p187.pdf Article Number: 50366 http://www.medicinaoral.com/odo/indice.htm © Medicina Oral S. L. C.I.F. B 96689336 - eISSN: 1989-5488 eMail: [email protected] Abstract Taurodontism can be defined as a change in tooth shape caused by the failure of Hertwig’s epithelial sheath dia- phragm to invaginate at the proper horizontal level. An enlarged pulp chamber, apical displacement of the pulpal floor, and no constriction at the level of the cemento-enamel junction are the characteristic features. Although per- manent molar teeth are most commonly affected, this change can also be seen in both the permanent and deciduous dentition, unilaterally or bilaterally, and in any combination of teeth or quadrants. -
Oral Manifestations in Patients with Glycogen Storage Disease: a Systematic Review of the Literature
applied sciences Review Oral Manifestations in Patients with Glycogen Storage Disease: A Systematic Review of the Literature 1, 1, 1 2 Antonio Romano y, Diana Russo y , Maria Contaldo , Dorina Lauritano , Fedora della Vella 3 , Rosario Serpico 1, Alberta Lucchese 1,* and Dario Di Stasio 1 1 Multidisciplinary Department of Medical-Surgical and Dental Specialties, University of Campania “L. Vanvitelli”, Via Luigi De Crecchio 6, 80138 Naples, Italy; [email protected] (A.R.); [email protected] (D.R.); [email protected] (M.C.); [email protected] (R.S.); [email protected] (D.D.S.) 2 Department of Medicine and Surgery, Centre of Neuroscience of Milan, University of Milano-Bicocca, 20126 Milan, Italy; [email protected] 3 Interdisciplinary Department of Medicine, University of Bari “A. Moro”, 70124 Bari, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-0815667670 Contributed equally to this article, so they are co-first authors. y Received: 28 August 2020; Accepted: 21 September 2020; Published: 25 September 2020 Abstract: (1) Background: Glycogen storage disease (GSD) represents a group of twenty-three types of metabolic disorders which damage the capacity of body to store glucose classified basing on the enzyme deficiency involved. Affected patients could present some oro-facial alterations: the purpose of this review is to catalog and characterize oral manifestations in these patients. (2) Methods: a systematic review of the literature among different search engines using PICOS criteria has been performed. The studies were included with the following criteria: tissues and anatomical structures of the oral cavity in humans, published in English, and available full text. -
Antibiotic Prophylaxis on Third Molar Extraction: Systematic Review of Recent Data
antibiotics Review Antibiotic Prophylaxis on Third Molar Extraction: Systematic Review of Recent Data Gabriele Cervino 1 , Marco Cicciù 1,* , Antonio Biondi 2, Salvatore Bocchieri 1, Alan Scott Herford 3, Luigi Laino 4 and Luca Fiorillo 1,4 1 Department of Biomedical and Dental Sciences, Morphological and Functional Images, School of Dentistry, University of Messina, 98100 Messina, Italy; [email protected] (G.C.); [email protected] (S.B.); lfi[email protected] (L.F.) 2 Department of General Surgery and Medical Surgery Specialties, University of Catania, 95100 Catania, Italy; [email protected] 3 Department of Maxillofacial Surgery, Loma Linda University, Loma Linda, CA 92354, USA; [email protected] 4 Multidisciplinary Department of Medical-Surgical and Odontostomatological Specialties, University of Campania “Luigi Vanvitelli”, 80121 Naples, Italy; [email protected] * Correspondence: [email protected] or [email protected] Received: 8 April 2019; Accepted: 30 April 2019; Published: 2 May 2019 Abstract: The aim of this paper was to highlight the most widely antibiotic protocols applied to the dental field, especially in the surgical treatment of impacted wisdom teeth. Once these protocols were screened, all the possible advantages or disadvantages for each drug and each posology were recorded in this review. In recent years, the need to use these protocols has been debated in the literature. The data obtained by this review underlined how antibiotic protocols applied to oral surgery treatments only included surgeries performed on patients who did not present other systemic pathologies. The first literature review obtained 140 results, and then after the application of the inclusion criteria, 12 papers were selected. -
Description Concept ID Synonyms Definition
Description Concept ID Synonyms Definition Category ABNORMALITIES OF TEETH 426390 Subcategory Cementum Defect 399115 Cementum aplasia 346218 Absence or paucity of cellular cementum (seen in hypophosphatasia) Cementum hypoplasia 180000 Hypocementosis Disturbance in structure of cementum, often seen in Juvenile periodontitis Florid cemento-osseous dysplasia 958771 Familial multiple cementoma; Florid osseous dysplasia Diffuse, multifocal cementosseous dysplasia Hypercementosis (Cementation 901056 Cementation hyperplasia; Cementosis; Cementum An idiopathic, non-neoplastic condition characterized by the excessive hyperplasia) hyperplasia buildup of normal cementum (calcified tissue) on the roots of one or more teeth Hypophosphatasia 976620 Hypophosphatasia mild; Phosphoethanol-aminuria Cementum defect; Autosomal recessive hereditary disease characterized by deficiency of alkaline phosphatase Odontohypophosphatasia 976622 Hypophosphatasia in which dental findings are the predominant manifestations of the disease Pulp sclerosis 179199 Dentin sclerosis Dentinal reaction to aging OR mild irritation Subcategory Dentin Defect 515523 Dentinogenesis imperfecta (Shell Teeth) 856459 Dentin, Hereditary Opalescent; Shell Teeth Dentin Defect; Autosomal dominant genetic disorder of tooth development Dentinogenesis Imperfecta - Shield I 977473 Dentin, Hereditary Opalescent; Shell Teeth Dentin Defect; Autosomal dominant genetic disorder of tooth development Dentinogenesis Imperfecta - Shield II 976722 Dentin, Hereditary Opalescent; Shell Teeth Dentin Defect; -
Cpac Summary – Paediatric Oral-Maxillofacial (Omf) Surgery
CPAC SUMMARY – PAEDIATRIC ORAL-MAXILLOFACIAL (OMF) SURGERY CLINICAL PRIORITY ACCESS CRITERIA Service Category: Clinic Type: Outpatient (1st Assessment) PAEDIATRIC ORAL-MAXILLOFACIAL (OMF) SURGERY Urgent Category Definitions: Semi-Urgent Routine If a patient presents to primary care with any of the following acute conditions, please contact the OMF Surgery consultant or registrar on call, for advice and transfer to Hospital Emergency Department: Immediate Examples (Not an exhaustive list) Treatment immediately or within 24 hours • Open and compound facial fracture including Le Fort I, II and III fractures of the • Significant or uncontrolled bleeding mid-face • Life threatening conditions • Multi-trauma victim with severe facial injury • Acute and significant functional impairment • Oral-facial trauma with potential to cause • Infection airway distress • Severe/acute oral medical conditions. • Potential airway compromise • Acute bilateral TMJ dislocation • Acute oral and facial sepsis • Ludwigs Angina • Large abscesses of the face or neck • Primary herpetic stomatitis • Stevens Johnson drug reaction • Pemphigus • Suspected malignancy • Congential problems with airway , feeding Urgent • Uncontrolled pain and speech problems • Uncontrolled oral • Ulcer in the mouth lasting longer than 10 infection/ulceration days • Oral/facial trauma not requiring • Oral/facial lumps/swellings increasing in size immediate treatment • Primary herpetic stomatitis • Acute unmanageable dental infection. • Pemphigus • Undisplaced fractures • Mandibular trismus