DOCSLIB.ORG

View the Program

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
View the Program Week at a Glance Hotel Floor Plan SUNDAY WEDNESDAY THURSDAY FRIDAY (cont.) April 19 April 22 April 23 April 24 4:00PM-7:00PM 6:30AM-6:30PM 6:30AM-6:00PM 10:30AM-12:00PM ACPA 72nd Annual Meeting Registration Registration Concurrent Session 1 & Pre-Conference Symposium 1- ASCFS 1 Registration Opens 7:00AM-8:00AM 7:00AM-8:00AM 2- Cleft Lip/Palate Surgery Eye Openers – Group 1 (1-4) Eye Openers – Group 2 (6-11) 3- Speech (separate ticket required) (separate ticket required) 4- Ortho/Dental MONDAY 5- Basic Research 7:00AM-1:00PM 7:00AM-6:00PM April 20 Poster Session A Poster Session C 12:00PM-1:30pm 7:30AM-5:30PM •Lunch Break (on your own) Registration 7:00AM-5:00PM 7:00AM-5:00PM • ASCFS Business Exhibits Open Exhibits Open Mtg/Luncheon* 9:00AM-5:30PM * open only to the members Pre-Conference Symposium: LOADING 7:30AM-8:20AM 8:00AM-10:00AM of ASCFS DOCK What is the “Ideal” Treatment Past Presidents’ Breakfast* Junior Investigator 7 3 Outcome for the Child with *open only to past presidents 12:00PM-3:00PM a Cleft? of ACPA and CPF 10:30AM-11:45AM ACPA Council AMBASSADOR BALLROOM (separate registration required) 6 2 General Session III Meeting/Luncheon 8:30AM-9:00AM PARKING 4 EAST PATIO 5 1 EAST FOYER Opening Ceremony 12:00PM-2:00PM 1:00PM-5:00PM WEST FOYER TUESDAY Annual Awards Luncheon Poster Session E 9:00AM-10:00AM April 21 W M AMBASSADOR FOYER 7:30AM-7:30PM Keynote Address: 2:30PM-4:00PM 1:30PM-3:00PM Harold Slavkin, DDS Concurrent Sessions 2 Registration Study Sessions – Group 1 (A-J) PATIO PATIO (separate ticket required) 6- ASCFS 2 8:00AM-11:30AM 10:30AM-12:30PM 7- Cleft Lip Palate Surgery 2 Pre-Conference Symposium: General Session I 4:30PM-6:00PM 8- Advances in BioImaging MOROCCAN Study Sessions – Group 2 (K-T) 9- Psychosocial FRONT BOARDROOM What is the “Ideal” Treatment MISSION HILLS Outcome for the Child with 12:30PM-2:00PM (separate ticket required) 10- Genetics BOARDROOM a Cleft? •Lunch Break (on your own) (separate registration required) • 2016 Program Committee 6:00PM-7:30PM 3:30PM-5:00PM CELEBRITY CELEBRITY Meeting/Luncheon Concurrent Session 3 PLAZA WEST PLAZA EAST MAIN CPF Donor Reception BUSINESS ENTRANCE 11- Mandible Microsomia POLO CENTER 8:00AM-12:00PM •Ethics Roundtable* (by invitation only) CELEBRITY FOYER ROOM ACPA Primer for Cleft Care (registration required) 12- Cleft Lip Palate Surgery 3 Providers* •Optional Lunch Available 12- Speech Surgery FRIDAY 14- Hospital Management F C M CELEBRITY W 1:30PM-6:30PM 15- Outcomes & International B A L L R O O M OASIS 12:00PM-1:00PM PATIO April 24 G B W OASIS BALLROOM *Optional Primer Lunch Poster Session B Issues RANCHO MISSION 7:00AM-5:30PM ED MIRAGE M OASIS HILLS FOYER FOYER MARKET 2:00PM-3:00PM Registration 6:30PM-10:30PM H A 12:00PM-1:30PM 5 3 & CAFE General II: Team Care Panel ACPA’s 72nd Annual Gala RANCHO ACPA/CPF Committee Chair 7:00AM-8:00AM OASIS WESTIN “Night at the Oasis” 642 COURTYARD WORKOUT Luncheons •ASCFS Breakfast RANCHO MIRAGE ROOM 3:00PM-6:30PM MIRAGE 7 1 1:30PM-6:30PM CPCJ Editorial Board LOADING Mtg/Dinner 7:00AM-3:30PM SATURDAY DOCK ACPA/CPF Committee Mtgs Exhibits Open (editor & section editors only) OASIS LOBBY EXECUTIVE April 25 DEN 5:00PM-6:00PM W OFFICES 3:15PM-4:45PM 8:00AM-12:30PM 7:30AM-10:00AM M New Member Orientation Poster Session D Registration MEETING PLANNERS FIRESIDE Discipline Forums OFFICE LOUNGE THE 6:30PM-8:30PM HIDEAWAY 5:00PM-6:45PM 8:00AM-9:00AM 7:30AM-9:30AM PINZIMINI ACPA/CPF Presidents’ Concurrent Panels Concurrent Sessions FIRE Welcoming Reception Ideas & Innovations* PIT (*upgraded Show & Tell) A: Quality of Life and Health D: First Year Care (7:30 - 8:30) Services E: Cleft Care in the Developing MASTERS B: Speech-Language Pathology World (8:30 - 9:30) PLAZA C. ASCFS Linton A. Whitaker F: ASCFS Panel: Timing of the Lecture: Craniosynostosis Surgical Management of Non- Syndromic Craniosynostosis 9:00AM-10:00AM (7:30 - 9:30) ACPA Annual Business Meeting (open only to members of ACPA) MEETING AJOURNED! This Program Belongs to: _______________________________________________________________________________________________ If found, please return to the ACPA registration desk. Thank you. Cover artwork designed by Amatullah King, Molly Brewer, and Hillary Jones. American Cleft Palate- Craniofacial Association 1 2015 Program Committee Robert J. Havlik, MD, Chair Amelia F. Drake, MD Patricia H. Glick, DMD, MS Bruce B. Horswell, MD, DDS, MS John N. Jensen, MD Joseph E. Losee, MD, ASCFS Liaison Judy A. Marciel, MSN, CPNP Michael S. Nelson, MD Jamie L. Perry, PhD, CCC-SLP Patricia A. Severns, MA Harold C. Slavkin, DDS Ronald Reed Hathaway, Marilyn A. Cohen, LSLP DDS, MS, MS CPF President Margot B. Stein, PhD ACPA President Michael J. VanLue, PhD, CCC-SLP Amatullah King, Staff Liaison 2015 Local Arrangements Committee Andrea O. Ray, MD, Chair Noreen Clarke, MSN, RN Katrina Dipple, MD, PhD Aaron M. Tanner, MS, CCC-SLP Yvonne R. Gutierrez, MD, Council Liaison Andrea O. Ray, MD Robert J. Havlik, MD Jessica Kokos, Staff Liaison Local Arrangements Chair ACPA Vice President and 2015 Program Chair National Office Staff Wendy-Jo Toyama, MBA, CAE, ACPA Executive Director Hillary Jones, Team Services Manager Amatullah King, Meetings Manager Jessica Kokos, Meetings Assistant Stephanie Williamson, MS, CPF Director of Family Services Annual Meeting Support Team ACPA/CPF National Office Staff and Support Team Tina Feliciano (l to r) – Wendy, Stephanie, Tina, Hillary, Sharon, Chinyere, Jessica, Amatullah Chinyere Harris Sharon Overcash Debbie Ogle, CPCJ Editorial Assistant Teri Jordan, CAE, CMP Allison Smith, CMP, Global Events Managers Kim Howard, CMP, Global Events Managers Debbie Teri Allison Kim 2 Table of Contents General Information. 3-4 ACPA Officers and Council Members . 5 ACPA Committee Members . 6 CPF Officers, Board of Directors, and Committee Members . 7 Cleft Palate-Craniofacial Journal Editorial Board . 8 ACPA and CPF Past Presidents . 9 ACPA and CPF Awards and Scholarships . 9 2015 Contributions to the Cleft Palate Foundation . 10-11 2014 Contributions to the Cleft Palate Foundation . 12-14 2014 American Cleft Palate-Craniofacial Association Financial Statements . 16 2014 Cleft Palate Foundation Financial Statements. 17 Pre-Conference Symposium I: What is the ‘Ideal’ Treatment Outcome for a Child With a Cleft Monday, April 20 & Tuesday, April 21 . 18-21 Symposium Faculty and Disclosures . 22-23 ACPA Primer for Cleft Care Providers Tuesday, April 21. 24-25 72nd Annual Meeting Scientific Program and Abstract Reference Tuesday, April 21 – Committee Meetings, Welcoming Reception, Eye Openers . 26 Wednesday, April 22 – Keynote Address, General Sessions . 27-30 Thursday, April 23 – Eye Openers, Junior Investigator, General Sessions, Discipline Forums, Study Sessions . 30-37 Friday, April 24 – Concurrent General and Specialty Sessions . 37-48 Saturday, April 25 – Concurrent General Sessions . 48 Poster Presentations . 49-55 Abstracts . 56-113 Authors Index. 114-117 Exhibits . 118-119 Summary of Events . 120-123 Hotel Layout . Inside Back Cover General lnformation 3 Registration and Information Eye Opener and Study Session speakers are responsible for Your ACPA registration and information desk is located in operating their own AV equipment. the Celebrity Ballroom foyer on the ground floor of the Westin Laser Pointers should be picked up by Session Co-Chairs just Mission Hills Hotel. Days and hours of operation are listed prior to their session and returned immediately afterwards to below. A message board has been provided for your the ACPA Registration Desk. convenience. Please check the board periodically for messages from other attendees or important telephone calls. Please All speakers must pick up their materials immediately have callers leave messages at your room if the messages are following their presentation. Do not leave them with the not urgent. technicians. ACPA and the AV staff will not accept responsibility for lost or damaged materials. Registration Desk Hours Journal Manuscripts Date Hours of Registration Manuscripts to be submitted to the Cleft Palate-Craniofacial Sunday, April 19 4:00PM - 7:00PM Journal should be left at the registration desk with an ACPA Monday, April 20 7:30AM - 5:30PM staff member to be given to Dr. Jack C. Yu, Editor. Tuesday, April 21 7:30AM - 7:30PM Wednesday, April 22 6:30AM - 6:30PM Poster Sessions, Exhibits and Coffee Breaks Thursday, April 23 6:30AM - 6:00PM Exhibits and posters will be displayed during the times specified Friday, April 24 7:00AM - 5:30PM in the Summary of Events. There will be five poster sessions: Saturday, April 25 7:30AM - 10:00AM Poster Sessions A and B will be on Wednesday, Session C on Thursday, and Sessions D and E on Friday. Poster sessions will Program, Badge, and Ticket Policy be held in the Celebrity Patio. All exhibits and coffee breaks will When you register, you will receive your badge as well as be held in the Celebrity Ballroom Foyer. appropriate tickets for social events, eye openers, and study sessions. If you are not attending the social event, please Welcome to New Members donate your tickets to students and residents. You may leave Look for the LIgHT BLUE RIBBON affixed to the badge of tickets with ACPA staff at the registration desk. individuals who have joined ACPA in the past year. Please take a It is essential that you keep your tickets with you for entrance moment to welcome them to ACPA and to introduce them to into each of the above short courses and social events. colleagues. Also, as you meet non-members (blue badges), you Volunteers will take your tickets at the doors.
Load more

Recommended publications
  • 59. Lateral Facial Clefts
    59 LATERAL FACIAL CLEFTS LI OR TRANSVERSE CLEFTS ARE CONSIDERED THE RESULT OF FAILURE OF MESODERM MIGRATION OR MERGING TO OBLITERATE MANDIBULAR THE EMBRYONIC GROOVES BETWEEN THE MAXILLARY AND PROMINENCES TRANSVERSE CLEFTS AS THESE CLEFTS ARE RARE AND ALMOST EVERYBODY HAVING ONE HAS AND REPORTED IT IT IS POSSIBLE TO REVIEW MOST OF THE REPORTED CASES 769 DESCRIBED THE AFTER WHEN NOTE TREATMENT SPECIFIC CASE RECORDINGS IN WHAT MAY SEEM HELTERSKELTER ARRANGEMENT GENERALIZATIONS MAY BE OF VALUE IN 1891 ROSE NOTED FOR LONG THE VERY EXISTENCE OF THIS MACROSROMATOUS DEFORMITY WAS DOUBTED BUT CASES HAVE BEEN RECOGNIZED MORE OR LESS SINCE 1715 WHEN MURALT PICTURED IT FOR THE FIRST TIME ONE OF THE FIRST CASES REPORTED WAS BY VROLIK WHOIN HIS 1849 CLEFTS WORK GAVE SEVERAL ILLUSTRATIONS OF COMMISSURAL AS WELL AS OTHER DEFORMITIES OF THE FACE OTHER CASES WERE REPORTED BY REISSMANN IN 1869 AND MORGAN IN 1882 MACROSTOMIA OR COMMISSURAL HARELIP ACCORDING TO ROSE IS DIAMETER OF WHICH EVIDENCED BY AN INCREASED THE MOUTH MAY VARY IN FROM SLIGHT INCREASE TO CONSIDERABLE DISTANCE CASE RE PORTED BY RYND IN 1862 THE MOUTH OPENING EXTENDED AS FAR AS THE THE LEFT FIRST MOLAR ON THE RIGHT SIDE AND TO THE LAST MOLAR ON IN 1887 SUTTON PUBLISHED THE DRAWING OF CHILD WITH VERY LARGE RED CICATRIX THIS CLEFT THE ANGLES OF WHICH GRADUALLY PASSED INTO SCAR ENDED IN GAPING WOUND OVER THE TEMPORAL REGION EXTEND ING TO THE DURA MATER ROSE ALSO POINTED OUT MACROSROMA IS NOR ONLY ATTENDED BY GREAT DISFIGUREMENT HUT IS ALSO TROU BLESOME FROM THE IMPOSSIBILITY OF THE CHILD RETAINING
    [Show full text]
  • OCSHCN-10G, Medical Eligibility List for Clinical and Case Management Services.Pdf
    OCSHCN-10g (01 2019) (Rev 7-15-2017) Office for Children with Special Health Care Needs Medical Eligibility List for Clinical and Case Management Services BODY SYSTEM ELIGIBLE DISEASES/CONDITIONS ICD-10-CM CODES AFFECTED AUTISM SPECTRUM Autistic disorder, current or active state F84.0 Autistic disorder DISORDER (ASD) F84.3 Other childhood disintegrative disorder Autistic disorder, residual state F84.5 Asperger’s Syndrome F84.8 Other pervasive developmental disorder Other specified pervasive developmental disorders, current or active state Other specified pervasive developmental disorders, residual state Unspecified pervasive development disorder, current or active Unspecified pervasive development disorder, residual state CARDIOVASCULAR Cardiac Dysrhythmias I47.0 Ventricular/Arrhythmia SYSTEM I47.1 Supraventricular/Tachycardia I47.2 Ventricular/Tachycardia I47.9 Paroxysmal/Tachycardia I48.0 Paroxysmal atrial fibrillation I48.1 Persistent atrial fibrillationar I48.2 Chronic atrial fibrillation I48.3 Typical atrial flutter I48.4 Atypical atrial flutter I49.0 Ventricular fibrillation and flutter I49.1 Atrial premature depolarization I49.2 Junctional premature depolarization I49.3 Ventricular premature depolarization I49.49 Ectopic beats Extrasystoles Extrasystolic arrhythmias Premature contractions Page 1 of 28 OCSHCN-10g (01 2019) (Rev 7-15-2017) Office for Children with Special Health Care Needs Medical Eligibility List for Clinical and Case Management Services I49.5 Tachycardia-Bradycardia Syndrome CARDIOVASCULAR Chronic pericarditis
    [Show full text]
  • MICHIGAN BIRTH DEFECTS REGISTRY Cytogenetics Laboratory Reporting Instructions 2002
    MICHIGAN BIRTH DEFECTS REGISTRY Cytogenetics Laboratory Reporting Instructions 2002 Michigan Department of Community Health Community Public Health Agency and Center for Health Statistics 3423 N. Martin Luther King Jr. Blvd. P. O. Box 30691 Lansing, Michigan 48909 Michigan Department of Community Health James K. Haveman, Jr., Director B-274a (March, 2002) Authority: P.A. 236 of 1988 BIRTH DEFECTS REGISTRY MICHIGAN DEPARTMENT OF COMMUNITY HEALTH BIRTH DEFECTS REGISTRY STAFF The Michigan Birth Defects Registry staff prepared this manual to provide the information needed to submit reports. The manual contains copies of the legislation mandating the Registry, the Rules for reporting birth defects, information about reportable and non reportable birth defects, and methods of reporting. Changes in the manual will be sent to each hospital contact to assist in complete and accurate reporting. We are interested in your comments about the manual and any suggestions about information you would like to receive. The Michigan Birth Defects Registry is located in the Office of the State Registrar and Division of Health Statistics. Registry staff can be reached at the following address: Michigan Birth Defects Registry 3423 N. Martin Luther King Jr. Blvd. P.O. Box 30691 Lansing MI 48909 Telephone number (517) 335-8678 FAX (517) 335-9513 FOR ASSISTANCE WITH SPECIFIC QUESTIONS PLEASE CONTACT Glenn E. Copeland (517) 335-8677 Cytogenetics Laboratory Reporting Instructions I. INTRODUCTION This manual provides detailed instructions on the proper reporting of diagnosed birth defects by cytogenetics laboratories. A report is required from cytogenetics laboratories whenever a reportable condition is diagnosed for patients under the age of two years.
    [Show full text]
  • Prevalence and Incidence of Rare Diseases: Bibliographic Data
    Number 1 | January 2019 Prevalence and incidence of rare diseases: Bibliographic data Prevalence, incidence or number of published cases listed by diseases (in alphabetical order) www.orpha.net www.orphadata.org If a range of national data is available, the average is Methodology calculated to estimate the worldwide or European prevalence or incidence. When a range of data sources is available, the most Orphanet carries out a systematic survey of literature in recent data source that meets a certain number of quality order to estimate the prevalence and incidence of rare criteria is favoured (registries, meta-analyses, diseases. This study aims to collect new data regarding population-based studies, large cohorts studies). point prevalence, birth prevalence and incidence, and to update already published data according to new For congenital diseases, the prevalence is estimated, so scientific studies or other available data. that: Prevalence = birth prevalence x (patient life This data is presented in the following reports published expectancy/general population life expectancy). biannually: When only incidence data is documented, the prevalence is estimated when possible, so that : • Prevalence, incidence or number of published cases listed by diseases (in alphabetical order); Prevalence = incidence x disease mean duration. • Diseases listed by decreasing prevalence, incidence When neither prevalence nor incidence data is available, or number of published cases; which is the case for very rare diseases, the number of cases or families documented in the medical literature is Data collection provided. A number of different sources are used : Limitations of the study • Registries (RARECARE, EUROCAT, etc) ; The prevalence and incidence data presented in this report are only estimations and cannot be considered to • National/international health institutes and agencies be absolutely correct.
    [Show full text]
  • Goldenhar Syndrome
    ndrom Sy es tic & e G n e e n G e f Saxena and David, J Genet Syndr Gene Ther 2012, 3:2 T o Journal of Genetic Syndromes h l e a r n a DOI: 10.4172/2157-7412.1000113 r p u y o J & Gene Therapy ISSN: 2157-7412 Case Report Open Access Goldenhar Syndrome - A Rare Case Report Runjhun Saxena1* and Maria Priscilla David2 1Department of Oral Medicine and Radiology, Karnavati School of Dentistry, Uvarsad, Gandhinagar, Gujarat 382422, India 2Department of Oral Medicine and Radiology, M R Ambedkar Dental College,1/36 Cline Road, Cooke Town, Bangalore-05, India Abstract Goldenhar syndrome or oculo-auriculovertebral (OAV) is a rare abnormality affecting the craniofacial region having extracranial manifestations as well. First described by Maurice Goldenhar, its etiology still remains uncertain. We describes a case of Goldenhar syndrome with craniofacial manifestations which makes it amenable to diagnosis by an oral physician. Keywords: Goldenhar syndrome; Mandibular hypoplasia; • Hands / Fingers: clubbing, polydactyly, clinodactyly, single Periauricular tags; Corneal opacities palmar crease Introduction • Vertebral column anomalies (atlas occipitalization, synosto- sis, hemivertebrae, fused vertebrae, scoliosis, and bifid spine) Franceschetti-Goldenhar syndrome or Goldenhar syndrome, also [4]. known as facioauriculovertebral spectrum (FAV), first and second branchial arch syndrome, or oculo-auriculovertebral (OAV) spectrum Principal deformities of the Goldenhar syndrome are often is a rare congenital malformation which encompasses various combined with various malformations, such as: morphological and functional abnormalities. The syndrome was first • Cleft lip and/or palate, tongue cleft, unilateral tongue recorded by German physician Carl Ferdinand Von Arlt in 1845, hypoplasia, and parotid gland aplasia.
    [Show full text]
  • The Status of Orofacial Cleft Care in Ghana
    The Status of Orofacial Cleft Care in Ghana Newman MA1, Agbenorku P2 1Department of Orthodontics and Pedodontics, University of Ghana Dental School, College of Health Sciences, University of Ghana, Accra, Ghana. 2Reconstructive Plastic Surgery & Burns Unit, Department of Surgery, Komfo Anokye Teaching Hospital, School of Medical Sciences, College of Health Sciences, Kwame Nkrumah University of Science & Technology, Kumasi, Ghana. Abstract Orofacial Clefts (OFC) are common congenital facial anomalies. The study seeks to determine the status of care for OFC patients in Ghana. Currently, in addition to the Ministry of Health, there are six Non-Governmental Organizations, which are dedicated to the provision of logistics for the management of cleft patients. As it is possible there could be OFC endemic areas in Ghana, sensitization of the population of the condition and management of this anomaly should be promoted. Persons of OFCs are faced with known challenges, which result in negative self-image that affect their quality of life. Hence educating the general public, in particular pregnant women who access antenatal care in health facilities may reduce ill effects associated with the anomaly. Genetic studies of the anomaly should also be encouraged to help decrease the incidence. Key Words: Orofacial Clefts, Care, Status, Non-Governmental Organization, Negative Self-image Introduction Effects and management Management of OFCs requires comprehensive approach from Incidence and predisposing factors professionals in specialties such as plastic surgery, maxillofacial, Orofacial cleft is one of the most common congenital abnormalities orthodontics, nursing, speech therapy and dental surgery among affecting people worldwide with high prevalence especially in others who work together and ensure quality care for the patients.
    [Show full text]
  • Doesrelative Maxillary Arch Worsen with Growthin Patients with Cleft Lip
    University of Dundee Does relative maxillary arch constriction worsen with growth in patients with Cleft lip and palate? Qureshi, Nafeesa; McIntyre, Grant; Mossey, Peter Published in: Journal of Cleft Lip Palate and Craniofacial Anomalies DOI: 10.4103/2348-2125.187510 Publication date: 2016 Licence: No Licence / Unknown Document Version Peer reviewed version Link to publication in Discovery Research Portal Citation for published version (APA): Qureshi, N., McIntyre, G., & Mossey, P. (2016). Does relative maxillary arch constriction worsen with growth in patients with Cleft lip and palate? A pilot study. Journal of Cleft Lip Palate and Craniofacial Anomalies, 3(2), 77- 82. https://doi.org/10.4103/2348-2125.187510 General rights Copyright and moral rights for the publications made accessible in Discovery Research Portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from Discovery Research Portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain. • You may freely distribute the URL identifying the publication in the public portal. Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 28. Sep. 2021 Original article Article title Does relative maxillary arch constriction worsen with growth in patients with Cleft lip and palate? A pilot study Running title Maxillary growth in CLP Authors N Qureshi N, MDSc.
    [Show full text]
  • Prof. Samia El-Azab 2017
    Prof. Samia El-Azab 2017 Developmental Disturbances of Oral and Para-oral tissues Intended Learning Outcomes (ILOs): By the end of these lectures every student will be able to: Recognize the normal development of oral and para-oral tissues Identify the developmental disturbances of oral and para-oral tissues Determine the pathogenesis of these developmental disturbances Describe the clinical significance of these developmental disturbances Normal development of face and lips: Nasal process descends from frontal bone forming 2 lateral nasal processes and one medial nasal process which is longer. Fusion occur between the lateral nasal processes and maxillary processes on both sides starting from the inner canthus of the eye and the median nasal process fuse with 2 maxillary process bilaterally to form the upper lip. The 2 mandibular process fuse in midline to form the lower lip. Developmental disturbances of the face I- Oblique facial cleft This is a developmental cleft start from the inner canthus of the eye to the ala of the nose or upper lip. It is due to failure of fusion between maxillary and lateral and medial nasal processes. It is usually unilateral but may be bilateral in about 20% of cases. II - Transverse facial cleft: This is a cleft running from the angle of the mouth towards the ear. It is due to failure of fusion between the maxillary and mandibular processes, and may be unilateral or bilateral, partial or complete (rare), extending from the angle of the mouth to the ear. III- Macrostomia and Microstomia: Macrostomia: it is an excessively large mouth. It is due to premature arrest of fusion between maxillary and mandibular processes bilaterally.
    [Show full text]
  • Back Matter 611-642.Pdf
    Index A Acrodysostosis, 527, 538 Aarskog syndrome, 527, 537 Acrofacial dysostosis 1, 580–581 differentiated from Opitz G/BBB Acrofacial dysplasia, 563 syndrome, 458 Acro-fronto-facio-nasal dysostosis Aase-Smith syndrome, 527 syndrome, 527, 538–539 Aase syndrome, 527, 537 Acromegaloid facial appearance Abducens nerve. See Cranial nerve VI syndrome, 527, 539 Abduction, Möbius sequence-related Acromegaloid phenotype-cutis verticis impairment of, 197, 198 gyrata-cornea leukoma, 527, 539 Abetalipoproteinemia, 527, 537 Acromesomelic dysplasia, Maroteaux- Ablepharon-macrostomia syndrome, Martinelli-Campailla type, 527, 527, 538 539 Abortion, spontaneous, chromosomal Acromicric dysplasia, 527, 539 abnormalities associated with, 83 Acro-osteolysis syndrome, 565 Abruzzo-Erickson syndrome, 527, 538 Acro-reno-ocular syndrome, 527, Acanthosis, 607 539 Acanthosis nigricans, Crouzon Acyclovir, 504, 505, 518 syndrome-related, 169 Adam complex, 207–209 Physician-parent interactions, Adams-Oliver syndrome, 527, 540 69–70 Adduction, Möbius sequence-related Acetyl-coenzyme A deficiency, 364 impairment of, 197, 198 N-Acetylcystine, 321 Adenoma sebaceum, tuberous sclerosis N-Acetyl galactosamine-4-sulfatase complex-related, 304, 308–309 deficiency, 366 Adrenocorticotropic hormone, 433 N-Acetyl galactosamine-6-sulfatase Aging, premature. See also Progeria deficiency, 357, 365 ataxia-telangiectasia-related, 320 a-N-Acetyl glucosaminidase acetyl Aglossia-adactyly syndrome, 584–585 transferase deficiency, 357 Agnathia-holoprosencephaly, 54 a-N-Acetyl glucosaminidase
    [Show full text]
  • 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;
    [Show full text]
  • Developmental Anomalies of the Temporomandibular Joint
    Developmental Anomalies of the Temporomandibular Joint R. Bruce Ross, DDS, MSc, FRCD he processes by which the human face develops in the Division of Orthodontics embryo are exceedingly complex, but they work out per- The Hospital for Sick Children fectly—-almost every time. Occasionally, however, the Toronto, Ontario, Canada T development of structures such as those comprising the temporo- mandibular articulation is disturbed, leading to an anomalous Professor Faoulty of Dentistry morphology in later life. It is important to note that an anomaly is University of Toronto not necessarily an undesirable condition requiring treatment. It Toronto, Ontario, Canada may be benign, with no associated problems, and therefore of no consequence; in fact, it may never be identified. Ross and Correspondence to: Johnston' have published a review of the developmental processes Dr R. B. Ross and etiology of undesirable conditions affecting the temporo- Faculty oS Dentistry mandibular joint (TMJ). University of Toronto Craniofacial anomalies may be caused by genetic faults (eg, 124 Edward Street Treacher Collins syndrome) or caused by a teratogenic agent (eg, Toronto, Ontario thahdomide), but most often it appears the cause is multifactorial M5G lG6 0anads Fax:416-813-6375 (eg, cleft hp and palate). When the entire human genome is avail- E-mail: [email protected] able and studied in persons with congenital anomalies, there may well be indicators for, or at least a demonstrable predisposition to, developmental problems. Problems involving the TMJ can be acquired or congenital (developmental). Tbe vast majority seen in a dental office are acquired dysfunctions, traumatic injuries, or pathologic condi- tions.
    [Show full text]
  • EUROCAT Syndrome Guide
    JRC - Central Registry european surveillance of congenital anomalies EUROCAT Syndrome Guide Definition and Coding of Syndromes Version July 2017 Revised in 2016 by Ingeborg Barisic, approved by the Coding & Classification Committee in 2017: Ester Garne, Diana Wellesley, David Tucker, Jorieke Bergman and Ingeborg Barisic Revised 2008 by Ingeborg Barisic, Helen Dolk and Ester Garne and discussed and approved by the Coding & Classification Committee 2008: Elisa Calzolari, Diana Wellesley, David Tucker, Ingeborg Barisic, Ester Garne The list of syndromes contained in the previous EUROCAT “Guide to the Coding of Eponyms and Syndromes” (Josephine Weatherall, 1979) was revised by Ingeborg Barisic, Helen Dolk, Ester Garne, Claude Stoll and Diana Wellesley at a meeting in London in November 2003. Approved by the members EUROCAT Coding & Classification Committee 2004: Ingeborg Barisic, Elisa Calzolari, Ester Garne, Annukka Ritvanen, Claude Stoll, Diana Wellesley 1 TABLE OF CONTENTS Introduction and Definitions 6 Coding Notes and Explanation of Guide 10 List of conditions to be coded in the syndrome field 13 List of conditions which should not be coded as syndromes 14 Syndromes – monogenic or unknown etiology Aarskog syndrome 18 Acrocephalopolysyndactyly (all types) 19 Alagille syndrome 20 Alport syndrome 21 Angelman syndrome 22 Aniridia-Wilms tumor syndrome, WAGR 23 Apert syndrome 24 Bardet-Biedl syndrome 25 Beckwith-Wiedemann syndrome (EMG syndrome) 26 Blepharophimosis-ptosis syndrome 28 Branchiootorenal syndrome (Melnick-Fraser syndrome) 29 CHARGE
    [Show full text]