Primary Tooth Eruption - an Ayurvedic Overview
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Pediatric Oral Pathology. Soft Tissue and Periodontal Conditions
PEDIATRIC ORAL HEALTH 0031-3955100 $15.00 + .OO PEDIATRIC ORAL PATHOLOGY Soft Tissue and Periodontal Conditions Jayne E. Delaney, DDS, MSD, and Martha Ann Keels, DDS, PhD Parents often are concerned with “lumps and bumps” that appear in the mouths of children. Pediatricians should be able to distinguish the normal clinical appearance of the intraoral tissues in children from gingivitis, periodontal abnormalities, and oral lesions. Recognizing early primary tooth mobility or early primary tooth loss is critical because these dental findings may be indicative of a severe underlying medical illness. Diagnostic criteria and .treatment recommendations are reviewed for many commonly encountered oral conditions. INTRAORAL SOFT-TISSUE ABNORMALITIES Congenital Lesions Ankyloglossia Ankyloglossia, or “tongue-tied,” is a common congenital condition characterized by an abnormally short lingual frenum and the inability to extend the tongue. The frenum may lengthen with growth to produce normal function. If the extent of the ankyloglossia is severe, speech may be affected, mandating speech therapy or surgical correction. If a child is able to extend his or her tongue sufficiently far to moisten the lower lip, then a frenectomy usually is not indicated (Fig. 1). From Private Practice, Waldorf, Maryland (JED); and Department of Pediatrics, Division of Pediatric Dentistry, Duke Children’s Hospital, Duke University Medical Center, Durham, North Carolina (MAK) ~~ ~ ~ ~ ~ ~ ~ PEDIATRIC CLINICS OF NORTH AMERICA VOLUME 47 * NUMBER 5 OCTOBER 2000 1125 1126 DELANEY & KEELS Figure 1. A, Short lingual frenum in a 4-year-old child. B, Child demonstrating the ability to lick his lower lip. Developmental Lesions Geographic Tongue Benign migratory glossitis, or geographic tongue, is a common finding during routine clinical examination of children. -
6 Development of the Teeth: Root and Supporting Structures Nagat M
AVERY Chap.06 27-11-2002 10:09 Pagina 108 108 II Development of the Teeth and Supporting Structures 6 Development of the Teeth: Root and Supporting Structures Nagat M. ElNesr and James K. Avery Chapter Outline Introduction Introduction... 108 Objectives... 108 Root development is initiated through the contributions Root Sheath Development... 109 of the cells originating from the enamel organ, dental Single-Root Formation... 110 papilla, and dental follicle. The cells of the outer enamel Multiple-Root Formation... 111 epithelium contact the inner enamel epithelium at the Root Formation Anomalies... 112 base of the enamel organ, the cervical loop (Figs. 6.1 and Fate of the Epithelial Root Sheath (Hertwig's Sheath)... 113 6.2A). Later, with crown completion, the cells of the cer- Dental Follicle... 114 vical loop continue to grow away from the crown and Development of (Intermediate) Cementum... 116 become root sheath cells (Figs. 6.2B and 6.3). The inner Cellular and Acellular Cementum... 116 root sheath cells cause root formation by inducing the Development of the Periodontal Ligament... 117 adjacent cells of the dental papilla to become odonto- Development of the Alveolar Process... 119 blasts, which in turn will form root dentin. The root Summary... 121 sheath will further dictate whether the tooth will have Self-Evaluation Review... 122 single or multiple roots. The remainder of the cells of the dental papilla will then become the cells of the root pulp.The third compo- nent in root formation, the dental follicle, is the tissue that surrounds the enamel organ, the dental papilla, and the root. -
Lecture 2 – Bone
Oral Histology Summary Notes Enoch Ng Lecture 2 – Bone - Protection of brain, lungs, other internal organs - Structural support for heart, lungs, and marrow - Attachment sites for muscles - Mineral reservoir for calcium (99% of body’s) and phosphorous (85% of body’s) - Trap for dangerous minerals (ex:// lead) - Transduction of sound - Endocrine organ (osteocalcin regulates insulin signaling, glucose metabolism, and fat mass) Structure - Compact/Cortical o Diaphysis of long bone, “envelope” of cuboid bones (vertebrae) o 10% porosity, 70-80% calcified (4x mass of trabecular bone) o Protective, subject to bending/torsion/compressive forces o Has Haversian system structure - Trabecular/Cancellous o Metaphysis and epiphysis of long bone, cuboid bone o 3D branching lattice formed along areas of mechanical stress o 50-90% porosity, 15-25% calcified (1/4 mass of compact bone) o High surface area high cellular activity (has marrow) o Metabolic turnover 8x greater than cortical bone o Subject to compressive forces o Trabeculae lined with endosteum (contains osteoprogenitors, osteoblasts, osteoclasts) - Woven Bone o Immature/primitive, rapidly growing . Normally – embryos, newborns, fracture calluses, metaphyseal region of bone . Abnormally – tumors, osteogenesis imperfecta, Pagetic bone o Disorganized, no uniform orientation of collagen fibers, coarse fibers, cells randomly arranged, varying mineral content, isotropic mechanical behavior (behavior the same no matter direction of applied force) - Lamellar Bone o Mature bone, remodeling of woven -
Basic Histology (23 Questions): Oral Histology (16 Questions
Board Question Breakdown (Anatomic Sciences section) The Anatomic Sciences portion of part I of the Dental Board exams consists of 100 test items. They are broken up into the following distribution: Gross Anatomy (50 questions): Head - 28 questions broken down in this fashion: - Oral cavity - 6 questions - Extraoral structures - 12 questions - Osteology - 6 questions - TMJ and muscles of mastication - 4 questions Neck - 5 questions Upper Limb - 3 questions Thoracic cavity - 5 questions Abdominopelvic cavity - 2 questions Neuroanatomy (CNS, ANS +) - 7 questions Basic Histology (23 questions): Ultrastructure (cell organelles) - 4 questions Basic tissues - 4 questions Bone, cartilage & joints - 3 questions Lymphatic & circulatory systems - 3 questions Endocrine system - 2 questions Respiratory system - 1 question Gastrointestinal system - 3 questions Genitouirinary systems - (reproductive & urinary) 2 questions Integument - 1 question Oral Histology (16 questions): Tooth & supporting structures - 9 questions Soft oral tissues (including dentin) - 5 questions Temporomandibular joint - 2 questions Developmental Biology (11 questions): Osteogenesis (bone formation) - 2 questions Tooth development, eruption & movement - 4 questions General embryology - 2 questions 2 National Board Part 1: Review questions for histology/oral histology (Answers follow at the end) 1. Normally most of the circulating white blood cells are a. basophilic leukocytes b. monocytes c. lymphocytes d. eosinophilic leukocytes e. neutrophilic leukocytes 2. Blood platelets are products of a. osteoclasts b. basophils c. red blood cells d. plasma cells e. megakaryocytes 3. Bacteria are frequently ingested by a. neutrophilic leukocytes b. basophilic leukocytes c. mast cells d. small lymphocytes e. fibrocytes 4. It is believed that worn out red cells are normally destroyed in the spleen by a. neutrophils b. -
Cell Proliferation Study in Human Tooth Germs
Cell proliferation study in human tooth germs Vanesa Pereira-Prado1, Gabriela Vigil-Bastitta2, Estefania Sicco3, Ronell Bologna-Molina4, Gabriel Tapia-Repetto5 DOI: 10.22592/ode2018n32a10 Abstract The aim of this study was to determine the expression of MCM4-5-6 in human tooth germs in the bell stage. Materials and methods: Histological samples were collected from four fetal maxillae placed in paraffin at the block archive of the Histology Department of the School of Dentistry, UdelaR. Sections were made for HE routine technique and for immunohistochemistry technique for MCM4-5-6. Results: Different regions of the enamel organ showed 100% positivity in the intermediate layer, a variation from 100% to 0% in the inner epithelium from the cervical loop to the incisal area, and 0% in the stellar reticulum as well as the outer epithelium. Conclusions: The results show and confirm the proliferative action of the different areas of the enamel organ. Keywords: MCM4, MCM5, MCM6, tooth germ, cell proliferation. 1 Molecular Pathology in Stomatology, School of Dentistry, Universidad de la República, Montevideo, Uruguay. ORCID: 0000-0001- 7747-671 2 Molecular Pathology in Stomatology, School of Dentistry, Universidad de la República, Montevideo, Uruguay. ORCID: 0000-0002- 0617-1279 3 Molecular Pathology in Stomatology, School of Dentistry, Universidad de la República, Montevideo, Uruguay. ORCID: 0000-0003- 1137-6866 4 Molecular Pathology in Stomatology, School of Dentistry, Universidad de la República, Montevideo, Uruguay. ORCID: 0000-0001- 9755-4779 5 Histology Department, School of Dentistry, Universidad de la República, Montevideo, Uruguay. ORCID: 0000-0003-4563-9142 78 Odontoestomatología. Vol. XX - Nº 32 - Diciembre 2018 Introduction that all the DNA is replicated (12), and prevents DNA from replicating more than once in the Tooth organogenesis is a process involving a same cell cycle (13). -
Effect of Posters and Mobile-Health Education Strategies on Teething Beliefs and Oral Health Knowledge Among Mothers in Nairobi
EFFECT OF POSTERS AND MOBILE-HEALTH EDUCATION STRATEGIES ON TEETHING BELIEFS AND ORAL HEALTH KNOWLEDGE AMONG MOTHERS IN NAIROBI. DR. REGINA MUTAVE JAMES REGISTRATION NUMBER: V91/96427/2014 Department of Periodontology/Community and Preventive Dentistry THESIS SUBMITTED IN FULFILMENT OF THE DOCTOR OF PHILOSOPHY DEGREE (PhD) IN COMMUNITY AND PREVENTIVE DENTISTRY, UNIVERSITY OF NAIROBI DECLARATION: I, Regina Mutave James hereby declare that this is my original work and that it has not been submitted by any other person for research purpose, degree or otherwise in any other university or institution. Signed ………………………………………. Date ………………………………. Regina Mutave James R.M.J PhD Thesis - 2015 Page i SUPERVISORS’ DECLARATION This research thesis has been submitted for the fulfillment of the requirement for the award of PhD in Community and Preventive Dentistry with our approval as supervisors. Supervisors: Signed ………………………………..Date……………………………. Prof. Loice W. Gathece BDS., MPH., PhD( Nbi). Department of Periodontology/ Community and Preventive Dentistry, University of Nairobi. Signed ………………………………..Date……………………………. Prof. Arthur M. Kemoli BDS (Nbi)., MSc (UvA)., PhD (UvA). Department of Pediatric Dentistry and Orthodontics, University of Nairobi. R.M.J PhD Thesis - 2015 Page ii DEDICATION To the Almighty, for His unending Grace! R.M.J PhD Thesis - 2015 Page iii ACKNOWLEDGEMENTS My PhD studies including this thesis were made possible by the financial support that I received from the University of Nairobi, and I am grateful for the opportunity. I wish to thank my supervisors Prof. Loice Gathece and Prof Arthur Kemoli who were always there to offer guidance and encouragement throughout the process. My sincere appreciation for my family and friends who stood by me even when I had no time for them and especially my children Erick, Aileen, Mbithe and Jynette. -
A Global Compendium of Oral Health
A Global Compendium of Oral Health A Global Compendium of Oral Health: Tooth Eruption and Hard Dental Tissue Anomalies Edited by Morenike Oluwatoyin Folayan A Global Compendium of Oral Health: Tooth Eruption and Hard Dental Tissue Anomalies Edited by Morenike Oluwatoyin Folayan This book first published 2019 Cambridge Scholars Publishing Lady Stephenson Library, Newcastle upon Tyne, NE6 2PA, UK British Library Cataloguing in Publication Data A catalogue record for this book is available from the British Library Copyright © 2019 by Morenike Oluwatoyin Folayan and contributors All rights for this book reserved. No part of this book may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without the prior permission of the copyright owner. ISBN (10): 1-5275-3691-2 ISBN (13): 978-1-5275-3691-3 TABLE OF CONTENTS Foreword .................................................................................................. viii Introduction ................................................................................................. 1 Dental Development: Anthropological Perspectives ................................. 31 Temitope A. Esan and Lynne A. Schepartz Belarus ....................................................................................................... 48 Natallia Shakavets, Alexander Yatzuk, Klavdia Gorbacheva and Nadezhda Chernyavskaya Bangladesh ............................................................................................... -
Initiation to Eruption
Head and Neck embryology Tooth Development Review head and neckblk embryology Initiation to eruption Skip Review Initiation Initiation stomodeum Epithelial cells (dental lamina) During 6th week, ectoderm in stomodeum forms horseshoe shaped mass of oral epithelium mesenchyme Basement membrane mesenchyme Initiation of anterior primary teeth Epithelial cells in horseshoe Dental lamina begins begins the sixth to seventh week form dental lamina growing into mesenchyme of development, initiation of additional At site where tooth will be teeth follows and continues for years Dental Lamina – Initiation Supernumerary tooth PREDICT what would happen if an extra tooth was initiated. Mesiodens 1 Bud Stage – eighth week Bud Stage Epithelium (dental Lamina) Dental lamina grows down into mesenchyme at site of tooth. Mesenchyme starts to change composition in response mesenchyme PREDICT what would happen if two tooth buds fused together or one tooth bud split in half. Fusion/Gemination Cap stage – week 9 By week 9, all germ layers of future tooth have formed ElEnamel organ (ename ll)l only) Dental papilla (dentin and pulp) Fusion Gemination Dental sac (cementum, PDL, Alveolar bone) PREDICT how you would know if it was mesenchyme fusion or gemination Cap Stage Successional Dental Lamina Each primary tooth germ has epithelium a successional lamina that becomes a permanent tooth Succedaneous teeth replace a deciduous tooth, nonsuccedaneous do not IDENTIFY nonsuccedaneous teeth mesenchyme PREDICT What occurs if no successional lamina forms? 2 Congenitally -
QUICK ORAL HEALTH FACTS ABOUT the YOUNG Dr Ng Jing Jing, Dr Wong Mun Loke
ORAL health IN PRIMARY CARE UNIT NO. 2 QUICK ORAL HEALTH FACTS ABOUT THE YOUNG Dr Ng Jing Jing, Dr Wong Mun Loke ABSTRACT Table 1. Eruption sequence of Primary Dentition This article sheds light on the sequence of teeth eruption Primary Upper Teeth Primary Lower Teeth in the young and teething problems; highlights the importance and functions of the primary dentition and Central Incisors: 8-13 months Central Incisors: 6-10 months provides a quick overview of common developmental Lateral Incisors: 8-13 months Lateral Incisors: 10-16 months dental anomalies and other dental conditions in Canines: 16-23 months Canines: 16-23 months children. First Molars: 16-23 months First Molars: 13-19 months Second Molars: 25-33 months Second Molars: 23-31 months SFP2011; 37(1) Supplement : 10-13 Table 2. Eruption sequence of Adult Dentition Adult Upper Teeth Adult Lower Teeth INTRODUCTION Central Incisors: 7-8 years Central Incisors: 6-7 years The early years are always full of exciting moments as we observe Lateral Incisors: 8-9 years Lateral Incisors: 7-8 years our children grow and develop. One of the most noticeable Canines: 11-12 years Canines: 9-10 years aspects of their growth and development is the eruption of First Premolars: 10-11 years First Premolars: 10-11 years teeth. The first sign of a tooth in the mouth never fails to Second Premolars: 11-12 years Second Premolars: 11-12 years attract the attention of the parent and child. For the parent, it First Molars: 6-7 years First Molars: 6-7 years marks an important developmental milestone of the child but Second Molars: 12-13 years Second Molars: 11-13 years for the child, it can be a source of irritation brought on by the Third Molars: 18-25 years Third Molars: 18-25 years whole process of teething. -
Observations on Continuously Growing Roots of the Sloth and the K14-Eda
EVOLUTION & DEVELOPMENT 10:2, 187–195 (2008) Observations on continuously growing roots of the sloth and the K14-Eda transgenic mice indicate that epithelial stem cells can give rise to both the ameloblast and root epithelium cell lineage creating distinct tooth patterns Mark Tummersà and Irma Thesleff1 Institute of Biotechnology, Viikki Biocenter, University of Helsinki, Finland ÃAuthor for correspondence (email: [email protected]) 1Current address and address at time of work for both authors: Institute of Biotechnology, P.O. Box 56, FIN-00014 University of Helsinki, Finland. SUMMARY Root development is traditionally associated that it acts as a functional stem cell niche. Similarly we show with the formation of Hertwig’s epithelial root sheath (HERS), that continuously growing roots represented by the sloth molar whose fragments give rise to the epithelial cell rests of and K14-Eda transgenic incisor maintain a cervical loop with a Malassez (ERM). The HERS is formed by depletion of the small core of stellate reticulum cells around the entire core of stellate reticulum cells, the putative stem cells, in the circumference of the tooth and do not form a HERS, and still cervical loop, leaving only a double layer of the basal give rise to ERM. We propose that HERS is not a necessary epithelium with limited growth capacity. The continuously structure to initiate root formation. Moreover, we conclude that growing incisor of the rodent is subdivided into a crown analog crown vs. root formation, i.e. the production of enamel vs. half on the labial side, with a cervical loop containing a large cementum, and the differentiation of the epithelial cells into core of stellate reticulum, and its progeny gives rise to enamel ameloblasts vs. -
AIPET Syllabus for Periodontology – Paper – II
Pravara Institute of Medical Sciences (Deemed University) All India Ph. D Entrance Test PIMS- AIPET Syllabus for Periodontology – Paper – II 1. APPLIED ANATOMY: Development of the Periodontium, Micro and Macro structural anatomy and biology of the periodontal tissues, Age changes in the periodontal tissues, Anatomy of the Periodontium: Macroscopic and microscopic anatomy, Blood supply of the Periodontium, Lymphatic system of the Periodontium, Nerves of the Periodontium • Temporomandibular joint, maxilla and mandible • Nerves of Periodontium. • Tongue, oropharynx • Muscles of mastication 2. PHYSIOLOGY : Blood, respiratory system --enumerate of the respiratory diseases which are a cause of periodontal diseases (periodontal medicine), Cardiovascular system: Blood pressure, normal ECG, shock • Endocrinology—hormonal influences on periodontium • Gastrointestinal system: Salivary secretion—composition, function & regulation Reproductive physiology • Hormones –Actions and regulations, role in periodontal disease • Nervous system: Pain pathways, Taste- buds, primary taste sensation & pathways for sensation 3. BIOCHEMISTRY: Basics of carbohydrartes, lipids, proteins, vitamins, enzymes and minerals, Diet and nutrition and Periodontium, Biochemical tests and their significance, Calcicum and phosphorus 4. PATHOLOGY: Cell structure and metabolism, Inflammation and repair, necrosis and degeneration, Immunity and hypersensitivity, Circulatory disturbances – edema, hemorrhage, shock, thrombosis, embolism, infarction and hypertension, Disturbances of -
Shh and Epithelial Growth and Polarity
Development 129, 5323-5337 5323 © 2002 The Company of Biologists Ltd doi:10.1242/dev.00100 Shh signaling within the dental epithelium is necessary for cell proliferation, growth and polarization Amel Gritli-Linde1,*, Marianna Bei2, Richard Maas2, Xiaoyan M. Zhang3, Anders Linde1 and Andrew P. McMahon4,* 1Department of Oral Biochemistry, Sahlgrenska Academy at Göteborg University, SE-405 30 Göteborg, Sweden 2Division of Genetics, Brigham and Women’s Hospital, Harvard Medical School, 20 Shattuck Street, Boston, MA 02115, USA 3Curis Inc., 45 Moulton Street, Cambridge, MA 02138, USA 4Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02135, USA *Authors for correspondence (e-mail: [email protected] and [email protected]) Accepted 12 August 2002 SUMMARY Sonic hedgehog (Shh), a member of the mammalian epithelium should block Shh signaling within dental Hedgehog (Hh) family, plays a key role during epithelial derivatives while preserving normal embryogenesis and organogenesis. Tooth development, mesenchymal signaling. Here we show that Shh-dependent odontogenesis, is governed by sequential and reciprocal interactions occur within the dental epithelium itself. The epithelial-mesenchymal interactions. Genetic removal of dental mesenchyme develops normally up until birth. In Shh activity from the dental epithelium, the sole source of contrast, dental epithelial derivatives show altered Shh during tooth development, alters tooth growth and proliferation, growth, differentiation and polarization.