Wormian Bone of the Orbit: a Case Report
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Anatomical Classification of Sutural Bones
MOJ Anatomy & Physiology Mini Review Open Access Anatomical classification of sutural bones Abstract Volume 3 Issue 4 - 2017 Sutural bones are accessory bones which occur within the skull. They get a different name, Rafael Romero Reverón1,2 derivative from the suture or sutures they are in contact with or with the centre of ossification 1Department of Human Anatomy, Universidad Central de or fontanel where they originate. They are classified into true Sutural bones and false Sutural Venezuela, Venezuela bones. True Sutural bones derived from one or many points of ossification. False Sutural 2Medical doctor Specialist in Orthopedic Trauma Surgery at bones are ossification centers not connected to independent bones. Although Sutural bones Centro Médico Docente La Trinidad, Venezuela they are poorly reported while they are quiet frequent. Sutural bones are being of interest to human anatomy, neurosurgery, physical anthropology, forensic medicine, craniofacial Correspondence: Rafael Romero Reverón, Department of surgery, radiology among others. Human Anatomy, Universidad Central de Venezuela, Medical doctor Specialist in Orthopedic Trauma Surgery at Centro Keywords: sutural bones, true sutural bones, false sutural bones, wormian bones, Médico Docente La Trinidad, Venezuela, anatomical classification Email [email protected] Received: February 23, 2017 | Published: April 10, 2017 Introduction both sexes as well as in both sides of the skull. Approximately half of Sutural bones are located in the lambdoid suture and fontanel and the The human skull is composed of several bones that fuse together masto-occipital suture. The second most common site of incidence after birth additionally to the regular centre of ossification of the skull. (about 25%) is in the coronal suture.7,8 The rest occur in any remaining Sutural bones are sporadically found in the course of cranial sutures sutures and fontanels.9 Knowledge of this variation is very important and fontanels or isolated. -
Subject Index
431 Subject Index 3D CT AIDS 348 articular disc 16 – normal bone anatomy of the face alcohol 425 articular tubercle (eminence) 16 and skull 2 allergic sinusitis 270 artificial bone chips 194 alveolar process 186 astrocytes 371 alveolar recess of maxillary sinus 4 astrocytoma 371 A ameloblastoma asymmetric tongue 315 – desmoplastic type 47 atlantoaxial dislocation 365 abscess 119, 335, 339, 376 – desmoplastic, mandible 55, 56 atrophy 249 – and cellulitis in parotid region 337 – mandible 57 – with fatty replacement – epidural 390 – solid/multicystic type 47 of medial pterygoid muscle 313 – in cheek 141 – solid/multicystic – with fatty replacement of most – in masticator space – – mandible 48, 49, 50 of the lateral pterygoid muscle 313 with intracranial spread 310 – – maxilla 48 autopsy specimen 147 – in middle cranial fossa 310 – unicystic type 47 avascular necrosis 154 – in parotid gland 336 – unicystic, mandible 51, 53 – parapharyngeal 138, 139, 140 amorphous calcification 363 – parenchymal 390 aneurysmal bone cyst 62 B – subdural 390 angiofollicular hyperplasia 388 – submandibular 137 angle of mandible 321 bacterial – subperiosteal 390 ankyloses 164 – infection 335 – thyroid 377 ankylosing spondylitis 160, 363 – meningitis 303 absence of zygoma 251 ankylosis 164, 165, 263 – rhinosinusitis 267 absent anorexia 369 ballooning 418, 420, 421 – zygoma 250 antegonial notching 251 base of tongue 4, 322, 324 – zygomatic arch 263 anterior band of articular disc 16 basket retrieval 418 absolute alcohol 425 anterior belly of digastric muscle 4 benign -
Pocket Atlas of Human Anatomy 4Th Edition
I Pocket Atlas of Human Anatomy 4th edition Feneis, Pocket Atlas of Human Anatomy © 2000 Thieme All rights reserved. Usage subject to terms and conditions of license. III Pocket Atlas of Human Anatomy Based on the International Nomenclature Heinz Feneis Wolfgang Dauber Professor Professor Formerly Institute of Anatomy Institute of Anatomy University of Tübingen University of Tübingen Tübingen, Germany Tübingen, Germany Fourth edition, fully revised 800 illustrations by Gerhard Spitzer Thieme Stuttgart · New York 2000 Feneis, Pocket Atlas of Human Anatomy © 2000 Thieme All rights reserved. Usage subject to terms and conditions of license. IV Library of Congress Cataloging-in-Publication Data is available from the publisher. 1st German edition 1967 2nd Japanese edition 1983 7th German edition 1993 2nd German edition 1970 1st Dutch edition 1984 2nd Dutch edition 1993 1st Italian edition 1970 2nd Swedish edition 1984 2nd Greek edition 1994 3rd German edition 1972 2nd English edition 1985 3rd English edition 1994 1st Polish edition 1973 2nd Polish edition 1986 3rd Spanish edition 1994 4th German edition 1974 1st French edition 1986 3rd Danish edition 1995 1st Spanish edition 1974 2nd Polish edition 1986 1st Russian edition 1996 1st Japanese edition 1974 6th German edition 1988 2nd Czech edition 1996 1st Portuguese edition 1976 2nd Italian edition 1989 3rd Swedish edition 1996 1st English edition 1976 2nd Spanish edition 1989 2nd Turkish edition 1997 1st Danish edition 1977 1st Turkish edition 1990 8th German edition 1998 1st Swedish edition 1979 1st Greek edition 1991 1st Indonesian edition 1998 1st Czech edition 1981 1st Chinese edition 1991 1st Basque edition 1998 5th German edition 1982 1st Icelandic edition 1992 3rd Dutch edtion 1999 2nd Danish edition 1983 3rd Polish edition 1992 4th Spanish edition 2000 This book is an authorized and revised translation of the 8th German edition published and copy- righted 1998 by Georg Thieme Verlag, Stuttgart, Germany. -
Genes in Eyecare Geneseyedoc 3 W.M
Genes in Eyecare geneseyedoc 3 W.M. Lyle and T.D. Williams 15 Mar 04 This information has been gathered from several sources; however, the principal source is V. A. McKusick’s Mendelian Inheritance in Man on CD-ROM. Baltimore, Johns Hopkins University Press, 1998. Other sources include McKusick’s, Mendelian Inheritance in Man. Catalogs of Human Genes and Genetic Disorders. Baltimore. Johns Hopkins University Press 1998 (12th edition). http://www.ncbi.nlm.nih.gov/Omim See also S.P.Daiger, L.S. Sullivan, and B.J.F. Rossiter Ret Net http://www.sph.uth.tmc.edu/Retnet disease.htm/. Also E.I. Traboulsi’s, Genetic Diseases of the Eye, New York, Oxford University Press, 1998. And Genetics in Primary Eyecare and Clinical Medicine by M.R. Seashore and R.S.Wappner, Appleton and Lange 1996. M. Ridley’s book Genome published in 2000 by Perennial provides additional information. Ridley estimates that we have 60,000 to 80,000 genes. See also R.M. Henig’s book The Monk in the Garden: The Lost and Found Genius of Gregor Mendel, published by Houghton Mifflin in 2001 which tells about the Father of Genetics. The 3rd edition of F. H. Roy’s book Ocular Syndromes and Systemic Diseases published by Lippincott Williams & Wilkins in 2002 facilitates differential diagnosis. Additional information is provided in D. Pavan-Langston’s Manual of Ocular Diagnosis and Therapy (5th edition) published by Lippincott Williams & Wilkins in 2002. M.A. Foote wrote Basic Human Genetics for Medical Writers in the AMWA Journal 2002;17:7-17. A compilation such as this might suggest that one gene = one disease. -
RD-Action Matchmaker – Summary of Disease Expertise Recorded Under
Summary of disease expertise recorded via RD-ACTION Matchmaker under each Thematic Grouping and EURORDIS Members’ Thematic Grouping Thematic Reported expertise of those completing the EURORDIS Member perspectives on Grouping matchmaker under each heading Grouping RD Thematically Rare Bone Achondroplasia/Hypochondroplasia Achondroplasia Amelia skeletal dysplasia’s including Achondroplasia/Growth hormone cleidocranial dysostosis, arthrogryposis deficiency/MPS/Turner Brachydactyly chondrodysplasia punctate Fibrous dysplasia of bone Collagenopathy and oncologic disease such as Fibrodysplasia ossificans progressive Li-Fraumeni syndrome Osteogenesis imperfecta Congenital hand and fore-foot conditions Sterno Costo Clavicular Hyperostosis Disorders of Sex Development Duchenne Muscular Dystrophy Ehlers –Danlos syndrome Fibrodysplasia Ossificans Progressiva Growth disorders Hypoparathyroidism Hypophosphatemic rickets & Nutritional Rickets Hypophosphatasia Jeune’s syndrome Limb reduction defects Madelung disease Metabolic Osteoporosis Multiple Hereditary Exostoses Osteogenesis imperfecta Osteoporosis Paediatric Osteoporosis Paget’s disease Phocomelia Pseudohypoparathyroidism Radial dysplasia Skeletal dysplasia Thanatophoric dwarfism Ulna dysplasia Rare Cancer and Adrenocortical tumours Acute monoblastic leukaemia Tumours Carcinoid tumours Brain tumour Craniopharyngioma Colon cancer, familial nonpolyposis Embryonal tumours of CNS Craniopharyngioma Ependymoma Desmoid disease Epithelial thymic tumours in -
Study of Wormian Bones on Dry Human Skull and Its Sexual Dimorphism in the Region of Andhra Pradesh
Original Research Article Study of Wormian Bones on Dry human skull and its sexual dimorphism in the region of Andhra Pradesh Shone Vasudeo Durge Assistant Professor, Dept. of Anatomy, Fathima Institute of Medical Sciences, Ramarajupalli, Andhra Pradesh Corresponding Author: E-mail: [email protected] Abstract This study was aimed at identifying the wormian bone and their overall incidence in respect to their number and location in the region of Andhra Pradesh. Overall incidence of wormian bones was more in female (47.72%) than in male skulls (41.66%). They occurred more frequently at lambdoid suture (38%). Wormian bones along the coronal suture, Bregma and Asterion were seen only in male skulls, while intra-orbital wormian bones and wormian bones at Pterion were seen only in female skulls. This study concludes by stating that, there exists a moderate degree of sexual dimorphism among the wormian bones with respect to overall incidence, number and location. Keywords- Skull, Sexual dimorphism, Wormian bones, Lambda, Asterion. Background knowledge of WBs is important in the diagnosis of Wormian bones, also known as intra-sutural bones, these disorders (Cremin, Goodman, Spranger et al., are extra bone pieces that occur within a suture in the 1982). It was reported that their incidence is well suited cranium. These are irregular isolated bones that appear for comparative studies as an anthropological marker or in addition to the usual centers of ossification of the an indicator of population distance (Gumusburun, cranium and, although unusual, are not rare. They occur Sevim, Katkici et al., 1997). Their knowledge is of most frequently in the course of the lambdoid suture, interest to the human anatomy, physical anthropology which is more tortuous than other sutures. -
Morphological and Topographical Study of Wormian Bones in Cadaver Dry Skulls
Original article Morphological and topographical study of Wormian bones in cadaver dry skulls Murlimanju, BV.*, Prabhu, LV., Ashraf, CM., Kumar, CG., Rai, R. and Maheshwari, C. Department of Anatomy, Manipal University, Centre for Basic Sciences, Kasturba Medical College, Mangalore, India *E-mail: [email protected] Abstract Introduction: The Wormian bones are formations associated with insufficient rate of suture closure and regarded as epigenetic and hypostotic traits. It was reported that there exists racial variability among the incidence of these bones. In the present study, the aims were to find the incidence of Wormian bones in Indian skulls and to analyze them topographically. Material and methods: The study included 78 human adult dry skulls of Indian population which were obtained from the neuroanatomy laboratory of our institution. They were macroscopically observed for the incidence and topographical distribution of the Wormian bones. Results: The Wormian bones were observed in 57 skulls (73.1%) of our series. Remaining 21 skulls (26.9%) didn’t show these variant bones. They were observed at the lambdoid suture in 56.4% cases (44 skulls; 14-bilateral; 18-right side; 12-left side), at the asterion in 17.9% (14 skulls; 3-bilateral; 2-right side; 9-left side), at the pterion in 11.5% (9 skulls; 4-right side; 5-left side), at the coronal suture in 1.3% (only one skull) and at the sagittal suture in 1.3% cases (only one skull). Conclusion: The current study observed Wormian bones in 73.1% of the cases from Indian population. This incidence rate is slightly higher compared to other reports and may be due to racial variations. -
Morfofunctional Structure of the Skull
N.L. Svintsytska V.H. Hryn Morfofunctional structure of the skull Study guide Poltava 2016 Ministry of Public Health of Ukraine Public Institution «Central Methodological Office for Higher Medical Education of MPH of Ukraine» Higher State Educational Establishment of Ukraine «Ukranian Medical Stomatological Academy» N.L. Svintsytska, V.H. Hryn Morfofunctional structure of the skull Study guide Poltava 2016 2 LBC 28.706 UDC 611.714/716 S 24 «Recommended by the Ministry of Health of Ukraine as textbook for English- speaking students of higher educational institutions of the MPH of Ukraine» (minutes of the meeting of the Commission for the organization of training and methodical literature for the persons enrolled in higher medical (pharmaceutical) educational establishments of postgraduate education MPH of Ukraine, from 02.06.2016 №2). Letter of the MPH of Ukraine of 11.07.2016 № 08.01-30/17321 Composed by: N.L. Svintsytska, Associate Professor at the Department of Human Anatomy of Higher State Educational Establishment of Ukraine «Ukrainian Medical Stomatological Academy», PhD in Medicine, Associate Professor V.H. Hryn, Associate Professor at the Department of Human Anatomy of Higher State Educational Establishment of Ukraine «Ukrainian Medical Stomatological Academy», PhD in Medicine, Associate Professor This textbook is intended for undergraduate, postgraduate students and continuing education of health care professionals in a variety of clinical disciplines (medicine, pediatrics, dentistry) as it includes the basic concepts of human anatomy of the skull in adults and newborns. Rewiewed by: O.M. Slobodian, Head of the Department of Anatomy, Topographic Anatomy and Operative Surgery of Higher State Educational Establishment of Ukraine «Bukovinian State Medical University», Doctor of Medical Sciences, Professor M.V. -
Appendix A: Organisation of a Craniofacial Unit
Appendix A: Organisation of a Craniofacial Unit The requirements of patients with craniofacial abnormalities are very complex and demand a multidisciplinary approach. Many body systems are affected, and every detail of patient management has to be given due attention. Care begins at birth and continues until the patient and his family have been relieved of the burden of the anomaly. A team is needed, capable of delivering expert patient care, and representative of all the relevant disciplines. Data, in the form of histories, physical examinations, and special investigations, are needed in planning treatment, and such data should be used to the maximum scientific effect, to improve present methods of management, still far from satisfactory, and to expand knowledge of the biology of cranial growth and its disorders. Craniofacial Units Sporadic craniofacial procedures performed by a surgeon on an irregular basis invite disaster. Tessier (1971a) estimated that each craniofacial centre should serve a population of 10 to 20 million people, provided that the team performed only craniofacial surgery and treated at least 50 new cases annually. As a consequence of Tessier's example and teaching there are now centres of acknowledged excellence in Paris and Nancy, attracting patients not only from France but also from North Africa and elsewhere. In North America there are now important craniofacial centres in Philadelphia, New York, Boston, Toronto, and Mexico City. Munro (1975) proposed that North America should be divided into seven regions, six for the United States and one for Canada, each serving populations of 20 to 40 million people. He believed that such centres would allow a concentration of multidisciplinary skills and accumulation of experience in the treatment of craniofacial anomalies. -
349 D.R. Laub Jr. (Ed.), Congenital Anomalies of the Upper
Index A dermatological anomalies , 182 Abductor digiti minimi (ADM) transfer , 102–103 skeletal abnormalities , 182 Abductor pollicis brevis (APB) , 186–187 upper extremity anomalies , 182, 183 ABS. See Amniotic band syndrome (ABS) visceral anomalies , 182 Achondroplasia defi nition of , 179 classifi cation/characterization , 338 description , 32, 33 defi nition of , 337–338 epidemiology of , 181 genetics , 338 genetics and embryology management , 338 molecular etiology , 180 Acrocephalosyndactyly syndrome , 32, 33, 179 prenatal diagnosis , 180–181 Acrosyndactyly repair, ABS , 300–302 molecular basis of , 180 Adactylic group IV symbrachydactyly , 129, 131 postoperative care and complications , 187 Al-Awadi syndrome , 154 treatment Amniotic band syndrome (ABS) APB release , 186–187 acrosyndactyly repair , 300–302 border digits syndactylies , 184 anesthesia concerns of fi rst web space release , 186 induction and maintenance of anesthesia , 43 patient age , 183 postoperative concerns , 43 secondary revisions , 187 preoperative preparation , 42–43 symphalangism , 184 classifi cation , 298 syndactyly ( see Syndactyly) clinical presentation thumb radial clinodactyly , 186–187 acrosyndactyly , 297–298 type II apert hand , 187–188 digital malformation , 297 Apical ectodermal ridge (AER) , 3–5 distal skeletal bones tapering , 297–298 Arthrogryposis , 210 hand deformity , 297 classic arthrogryposis , 305–306, 308 complications , 302 classifi cation , 305, 306 constriction band release defi nition of , 229, 230, 305 Upton’s technique , 299, 301 de-rotation osteotomy, shoulder , 308, 309 z-plasty , 299–300 distal , 230–231 ( see Distal arthrogryposis) diagnosis of , 296 elbow treatment digital hypoplasia reconstruction , 302 muscle transfers , 310–311 etiology of , 295–296 nonoperative management , 308 preoperative considerations , 299 posterior elbow capsular release , 309 treatment , 299 radial head dislocations , 311 Amniotic constriction band syndrome. -
Molecular Mechanisms in Calvarial Bone and Suture Development
Molecular Mechanisms in Calvarial Bone and Suture Development David Rice Department of Orthodontics and Pedodontics, Institute of Dentistry, and, Developmental Biology Programme, Institute of Biotechnology, University of Helsinki, Finland. Academic Dissertation To be discussed publicly with the permission of the Faculty of Medicine of the University of Helsinki, in auditorium 1041, Viikki Biocenter 2 on 5th November 1999, at 12 noon. Helsinki 1999 Supervised by: Professor Irma Thesleff, University of Helsinki, Finland. Reviewed by: Professor Seppo Vainio, University of Oulu, Finland. and Professor Kalervo Väänänen, University of Turku, Finland. Opponent: Assistant Professor Lynne Opperman, Baylor School of Dentistry, Texas A & M University, U.S.A. ISBN 951-45-8960-2 (PDF version) Helsinki 1999 Helsingin yliopiston verkkojulkaisut http://ethesis.helsinki.fi/ 2 CONTENTS 3DJH /LVW RI 2ULJLQDO 3XEOLFDWLRQV 5 $EEUHYLDWLRQV 6 6XPPDU\ 7 5HYLHZ RI WKH /LWHUDWXUH 9 %RQH 'HYHORSPHQW DQG *URZWK 9 Origin and patterning of the craniofacial skeleton 9 Mesenchymal condensations 9 Intramembraneous ossification 10 Endochondral ossification 11 &HOOXODU %LRORJ\ RI %RQH 11 Osteoblasts, stromal cells and osteocytes 13 Osteoclasts 18 Proliferation of bone cells 22 Proliferation during calvarial bone and suture development 22 Apoptosis during embryogenesis 23 Apoptosis during bone and suture development 24 'HYHORSPHQW RI WKH &DOYDULD 24 Developmental anatomy 24 Sutures and fontanelles 25 Suture morphology 26 Suture closure 27 Suture position 27 Sutural growth -
Atlas of the Facial Nerve and Related Structures
Rhoton Yoshioka Atlas of the Facial Nerve Unique Atlas Opens Window and Related Structures Into Facial Nerve Anatomy… Atlas of the Facial Nerve and Related Structures and Related Nerve Facial of the Atlas “His meticulous methods of anatomical dissection and microsurgical techniques helped transform the primitive specialty of neurosurgery into the magnificent surgical discipline that it is today.”— Nobutaka Yoshioka American Association of Neurological Surgeons. Albert L. Rhoton, Jr. Nobutaka Yoshioka, MD, PhD and Albert L. Rhoton, Jr., MD have created an anatomical atlas of astounding precision. An unparalleled teaching tool, this atlas opens a unique window into the anatomical intricacies of complex facial nerves and related structures. An internationally renowned author, educator, brain anatomist, and neurosurgeon, Dr. Rhoton is regarded by colleagues as one of the fathers of modern microscopic neurosurgery. Dr. Yoshioka, an esteemed craniofacial reconstructive surgeon in Japan, mastered this precise dissection technique while undertaking a fellowship at Dr. Rhoton’s microanatomy lab, writing in the preface that within such precision images lies potential for surgical innovation. Special Features • Exquisite color photographs, prepared from carefully dissected latex injected cadavers, reveal anatomy layer by layer with remarkable detail and clarity • An added highlight, 3-D versions of these extraordinary images, are available online in the Thieme MediaCenter • Major sections include intracranial region and skull, upper facial and midfacial region, and lower facial and posterolateral neck region Organized by region, each layered dissection elucidates specific nerves and structures with pinpoint accuracy, providing the clinician with in-depth anatomical insights. Precise clinical explanations accompany each photograph. In tandem, the images and text provide an excellent foundation for understanding the nerves and structures impacted by neurosurgical-related pathologies as well as other conditions and injuries.