Embryology8 Dr.Ban Facial, Nasal and Palatal Development the External Human Face Develops Between the 4Th and 6Th Weeks of Embryonic Development
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Syndromes of the First and Second Branchial Arches, Part 1: Embryology and Characteristic REVIEW ARTICLE Defects
Syndromes of the First and Second Branchial Arches, Part 1: Embryology and Characteristic REVIEW ARTICLE Defects J.M. Johnson SUMMARY: A variety of congenital syndromes affecting the face occur due to defects involving the G. Moonis first and second BAs. Radiographic evaluation of craniofacial deformities is necessary to define aberrant anatomy, plan surgical procedures, and evaluate the effects of craniofacial growth and G.E. Green surgical reconstructions. High-resolution CT has proved vital in determining the nature and extent of R. Carmody these syndromes. The radiologic evaluation of syndromes of the first and second BAs should begin H.N. Burbank first by studying a series of isolated defects: CL with or without CP, micrognathia, and EAC atresia, which compose the major features of these syndromes and allow more specific diagnosis. After discussion of these defects and the associated embryology, we proceed to discuss the VCFS, PRS, ACS, TCS, Stickler syndrome, and HFM. ABBREVIATIONS: ACS ϭ auriculocondylar syndrome; BA ϭ branchial arch; CL ϭ cleft lip; CL/P ϭ cleft lip/palate; CP ϭ cleft palate; EAC ϭ external auditory canal; HFM ϭ hemifacial microsomia; MDCT ϭ multidetector CT; PRS ϭ Pierre Robin sequence; TCS ϭ Treacher Collins syndrome; VCFS ϭ velocardiofacial syndrome adiographic evaluation of craniofacial deformities is nec- major features of the syndromes of the first and second BAs. Ressary to define aberrant anatomy, plan surgical proce- Part 2 of this review discusses the syndromes and their radio- dures, and evaluate the effects of craniofacial growth and sur- graphic features: PRS, HFM, ACS, TCS, Stickler syndrome, gical reconstructions.1 The recent rapid proliferation of and VCFS. -
Uvula in Snoring and Obstructive Sleep Apnea: Role and Surgical Intervention
Opinion American Journal of Otolaryngology and Head and Neck Surgery Published: 13 Apr, 2020 Uvula in Snoring and Obstructive Sleep Apnea: Role and Surgical Intervention Elbassiouny AM* Department of Otolaryngology, Cairo University, Egypt Abstract Objective: Currently, the consideration of the enlarged uvula as a cause of snoring and Obstructive Sleep Apnea (OSA) lacks data for objective interpretation. This article focused on some concepts on how we can manage the enlarged uvula in cases of snoring and OSA. The purpose of the present article is to discuss the cost benefits of uvular surgery versus its preservation. Conclusion: The direct correlation between the uvula and OSA needs to be reevaluated to maintain a balance between reserving its anatomical and physiological functions and surgically manipulating it as a part of palatopharyngeal surgery, yet further objective studies are needed to reach optimal results. Keywords: Uvula; Snoring; Obstructive sleep apnea Introduction The palatine uvula, usually referred to as simply the uvula, is that part of the soft palate that has an anatomical structure and serves some functions. Anatomically, the uvula, a conic projection from the back edge of the middle of the soft palate, is composed of connective tissue containing several racemose glands, and some muscular fibers, musculus uvulae muscle; arises from the posterior nasal spine and the palatine aponeurosis and inserts into the mucous membrane of the uvula. It contains many serous glands, which produce thin saliva [1]. Physiologically, the uvula serves several functions. First during swallowing, the soft palate and the uvula move together to close off the nasopharynx OPEN ACCESS and prevent food from entering the nasal cavity. -
Illustrated Review of the Embryology and Development of the Facial
REVIEW ARTICLE Illustrated Review of the Embryology and Development of the Facial Region, Part 2: Late Development of the Fetal Face and Changes in the Face from the Newborn to Adulthood P.M. Som and T.P. Naidich ABSTRACT SUMMARY: The later embryogenesis of the fetal face and the alteration in the facial structure from birth to adulthood have been reviewed. Part 3 of the review will address the molecular mechanisms that are responsible for the changes described in parts 1 and 2. art 1 of this 3-part review primarily dealt with the early em- first make contact, each is completely covered by a homoge- Pbryologic development of the face and nasal cavity. Part 2 will neous epithelium. A special epithelium arises at the edge of discuss the later embryonic and fetal development of the face, and each palatal shelf, facilitating the eventual fusion of these changes in facial appearance from neonate to adulthood will be shelves. The epithelium on the nasal cavity surface of the palate reviewed. will differentiate into columnar ciliated epithelium. The epi- thelium on the oral cavity side of the palate will differentiate Formation of the Palate into stratified squamous epithelium. Between the sixth and 12th weeks, the palate is formed from 3 The 2 palatal shelves also fuse with the triangular primary pal- primordia: a midline median palatine process and paired lateral ate anteromedially to form a y-shaped fusion line. The point of palatine processes (Fig 1). In the beginning of the sixth week, fusion of the secondary palatal shelves with the primary palate is merging of the paired medial nasal processes forms the intermax- marked in the adult by the incisive foramen. -
EMBRYOLOGY7 Dr.Ban A.Ghani Developmdent of External
EMBRYOLOGY7 Dr.Ban A.Ghani EMBRYOLOGY7 Dr.Ban A.Ghani Developmdent of external /Sequence of developmental During the third week of development an oropharyngeal membrane buccopharyngeal , or oral membrane) is first seen at the site of the future face, between the primordium of the heart and the rapidly enlarging primordium of the brain. It is composed of ectoderm externally and endoderm internally. It lies at the beginning of the digestive tract and breaks down during the 4th week in order to form the opening between the future oral cavity (primitive mouth or stomodeum) and the foregut. The oropharyngeal membrane breaks down when it stops growing. While tissues around it expand very rapidly, the oropharyngeal membrane’s non-proliferating cells are gradually pulled apart because they cannot fill the expanding area. The human face begins to form during the 4th week of embryonic development. By the 6th week the external face is completed. The development of the palate subdivides nasal and oral cavities. This development continues into the 12th week with completion of the soft palate. Human face during the 4th prenatal week. Around the centrally located oral pit are grouped the frontal and maxillary processes and the mandibular arch. 1 EMBRYOLOGY7 Dr.Ban A.Ghani Human face during the 5th prenatal week. The nasal pits develop and appear on the sides of the face. The frontal process now becomes the frontonasal process Human face during the 6th prenatal week. Nasal pits appear more centrally located in the medial nasal process. This is the result of growth of the lateral face, which also causes the eyes to approach the front of the face. -
A New Origin for the Maxillary Jaw
Developmental Biology 276 (2004) 207–224 www.elsevier.com/locate/ydbio A new origin for the maxillary jaw Sang-Hwy Leea, Olivier Be´dardb,1, Marcela Buchtova´b, Katherine Fub, Joy M. Richmanb,* aDepartment of Oral, Maxillofacial Surgery and Oral Science Research Center, Medical Science and Engineering Research Center, BK 21 Project for Medical Science, College of Dentistry Yonsei University, Seoul, Korea bDepartment of Oral Health Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC, Canada, V6T 1Z3 Received for publication 7 April 2004, revised 5 August 2004, accepted 31 August 2004 Available online 5 October 2004 Abstract One conserved feature of craniofacial development is that the first pharyngeal arch has two components, the maxillary and mandibular, which then form the upper and lower jaws, respectively. However, until now, there have been no tests of whether the maxillary cells originate entirely within the first pharyngeal arch or whether they originate in a separate condensation, cranial to the first arch. We therefore constructed a fate map of the pharyngeal arches and environs with a series of dye injections into stage 13–17 chicken embryos. We found that from the earliest stage examined, the major contribution to the maxillary bud is from post-optic mesenchyme with a relatively minor contribution from the maxillo-mandibular cleft. Cells labeled within the first pharyngeal arch contributed exclusively to the mandibular prominence. Gene expression data showed that there were different molecular codes for the cranial and caudal maxillary prominence. Two of the genes examined, Rarb (retinoic acid receptor b) and Bmp4 (bone morphogenetic protein) were expressed in the post-optic mesenchyme and epithelium prior to formation of the maxillary prominence and then were restricted to the cranial half of the maxillary prominence. -
Facial and Palatal Development
11. FACIAL AND PALATAL DEVELOPMENT Letty Moss-Salentijn DDS, PhD Dr. Edwin S.Robinson Professor of Dentistry (in Anatomy and Cell Biology) E-mail: [email protected] READING ASSIGNMENT: Larsen 3rd edition: p.352; pp.365-371; 398-404. SUMMARY: The external human face develops between the 4th and 6th weeks of embryonic development. Facial swellings arise on the frontonasal process (2 medial nasal and 2 lateral nasal processes) and the first pharyngeal arch (2 mandibular and 2 maxillary processes). By a process of merging and some localized fusion these processes come together to form the continuous surfaces of the external face. The primary palate is formed in this period by fusion/merging of the medial nasal and maxillary processes. Subsequently, between 6th and 12th embryonic/fetal weeks, the secondary palate is formed as the result of fusion between palatal processes growing from the oral surfaces of the maxillary processes. Each merging and fusion site is also the site of a potential facial or palatal cleft. LEARNING OBJECTIVES You should be able to: a. Demonstrate on a frontal image of a human face those parts of the face that are formed by contributions from the frontonasal process and those that are formed by contributions from the first pharyngeal arch. b. Describe the following as to site, composition, time of appearance, and fate: oropharyngeal membrane, oronasal membrane. c. List the derivatives of the four pairs of facial processes and the pair of palatal processes. d. Describe the development of the nose and primary palate. e. Explain the differences between the processes of merging and fusion. -
A Case of Pharynx Syphilis at Secondary Stage
Case Report Annals of Clinical Case Reports Published: 03 Mar, 2017 A Case of Pharynx Syphilis at Secondary Stage XU Wen, YU Shaoqing* and JIN Ling Department of Otolaryngology, Tongji Hospital, Tongji University Abstract A 48-year-old female patient had throat discomfort and slightly pain for three month. Her symptom was getting aggravated and repetitive after being misdiagnosed with acute tonsillitis. Later, we found patient’s mucous membrane of double tonsil, palatoglossus arch, palatopharyngeus arch, palatine uvula was covered by white pseudo-membrane. It was suspected as syphilis of the pharynx. Rapid Plasma Reagin (RPR) and Treponema Pallidum Hemagglutination Assay (TPHA) tests confirmed the pharynx syphilis. After the patient went through the anti-syphilitic remedy, her symptoms and signs completely disappeared. During the 24-month routinely follow-up, no relapse was observed and the pharynx lesion disappear accompany with negative RPR tests results. Keywords: Pharynx; Syphilis; Secondary syphilis Introduction Syphilis is a sexually transmitted disease caused by the spirochete Treponema pallidum. Syphilis could affect any human organs and tissues and trigger various manifestations. The incubation period of Treponema pallidum is between 15 and 90 days. Recently, the incidence of syphilis is increased rapidly in China, and it is ranked number three among infectious diseases in China, only preceded by tuberculosis and hepatitis. China economy development, imbalance of male and female population, emergence of numerous migrant workers from rural area, the social acceptance of sexual services, and the growth in number of male homosexuality are the major attributions to the increase in incidence rate of syphilis [1]. Such incidence rate grew from 6.43 percent of every one hundred thousand population in 2000 to 32.86 percent in 2013 [2]. -
Co-Relation of Clinical and Histologic Grade with Soft Palate Morphology in Oral Submucous Fibrosis Patients: a Histologic and Cephalometric Study
_______________________________________________________________________ORIGINAL RESEARCH Co-relation of clinical and histologic grade with soft palate morphology in oral submucous fibrosis patients: A histologic and cephalometric study Tekchandani V1, Thakur M2, Palve D3, Mohale D4, Gupta R5 ABSTRACT 1,4,5Postgraduate student, Dept. of Introduction: Oral submucous fibrosis (OSMF) is a chronic progressive Oral Pathology and Microbiology, precancerous condition with an alarming prevalence in India. Prevention and early Swargiya Dadasaheb Kalmegh diagnosis of this condition can not only nip it in the bud, but also curb the menace Smruti Dental College and Hospital, of malignant transformation of this disease. OSMF is believed to produce fibrotic Nagpur changes beginning in the soft palate and faucial pillars, progressing anteriorly in 2Professor and Head, Dept. of Oral Pathology and Microbiology, the oral cavity. Swargiya Dadasaheb Kalmegh Aim: The present study was carried out to evaluate and correlate the morphology Smruti Dental College and Hospital, of soft palate in Oral submucous fibrosis (OSMF) patients to the clinical and Nagpur histopathologic grade, using digital lateral cephalogram. 3Professor, Dept. of Oral Pathology Method: A total of 80 patients (40 OSMF and 40 Control) were evaluated for soft and Microbiology, Swargiya palatal morphology. The antero-posterior and supero-inferior dimensions of soft Dadasaheb Kalmegh Smruti Dental palate were measured on digital lateral cephalogram, categorized as Type 1 to Type College and Hospital, Nagpur 6 and were then compared to clinical and histopathologic grade. Results: In our study, Type 1 (leaf-shaped) soft palate was found to be the most common followed by Type 6 (crook-shaped) and Type 3 (butt-like) varieties. -
Cavitas Oris) Is the Initial Part of the Alimentary Or Digestive Tract
ANATOMY AND HISTOLOGY OF THE ORAL CAVITY The oral cavity (cavitas oris) is the initial part of the alimentary or digestive tract. It is boarded by lips on the front, by cheeks on the sides, by the hard and soft palates at the top, by pharynx at the back part and by the mouth bottom at the bottom. 1. Upper lip 7. Tongue 2. Upper gum 8. Mandible teeth 3. Upper-jaw-teeth 9. Lower gum 4. Hard palate 10. Lower lip 5. Soft palate uvula 11. Cheek 6. Tonsils The oral cavity is a combination of organs and tissues performing a set of functions: 1. Chewing – performed by teeth 2. Speaking – a process with participation of tongue, teeth, lips and the palates 3. Digestive - due to enzymes of saliva deconstruction of some substance takes place in the oral cavity, and the permeability of mucous membrane helps to absorb the stuff. 4. Protecting - is performed with the help of some substances and cells, existing in the saliva (lysozyme, interferon, leucocyte, etc.), as well as by selective permeability of the epithelium of mucous membrane. Tonsils also have great importance in the provision of this function (palatal, pharyngeal, lingual). 5. Sensitive - feeling of pain, as well as felling of taste and tactile feeling are provided by big amount of receptors and taste sensitive papilla of mucous membrane of oral cavity. The oral cavity is divided by teeth arch into 2 parts: a. frontal or vestibular part of the mouth (vestibulum oris), which is the space between lips and cheeks from outside and teeth and gingiva from inside. -
AP-2-Null Cells Disrupt Morphogenesis of the Eye, Face, and Limbs in Chimeric Mice
Proc. Natl. Acad. Sci. USA Vol. 95, pp. 13714–13719, November 1998 Developmental Biology AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice TIMOTHY NOTTOLI*, STEPHANIE HAGOPIAN-DONALDSON*, JIAN ZHANG*, ARCHIBALD PERKINS*†, AND TREVOR WILLIAMS*‡ *Department of Molecular, Cellular, and Developmental Biology, Yale University, 266 Whitney Avenue, New Haven, CT 06511; and †Department of Pathology, Yale University School of Medicine, New Haven, CT 06510 Communicated by Francis H. Ruddle, Yale University, New Haven, CT, August 28, 1998 (received for review January 15, 1998) ABSTRACT The homozygous disruption of the mouse dent developmental programs are probably regulated by AP-2. AP-2 gene yields a complex and lethal phenotype that results Therefore, we adopted an approach that enabled independent from defective development of the neural tube, head, and body developmental defects to be obtained in isolation. This strat- wall. The severe and pleiotropic developmental abnormalities egy relied on the generation of chimeric mice composed of observed in the knockout mouse suggested that AP-2 may both wild-type (wt) and AP-2-null cells; when a phenotype regulate several morphogenic pathways. To uncouple the results from the interaction of multiple independent develop- individual developmental mechanisms that are dependent on mental defects, an individual chimera will display particular AP-2, we have now analyzed chimeric mice composed of both aspects of the pathology depending on the distribution of the wild-type and AP-2-null cells. The phenotypes obtained from AP-2-null cells. A second consideration behind the generation these chimeras indicate that there is an independent require- of chimeras was to determine whether the severity of the KO ment for AP-2 in the formation of the neural tube, body wall, phenotype concealed more subtle requirements for AP-2 in and craniofacial skeleton. -
Msx Homeobox Gene Family and Craniofacial Development
Cell research (2003); 13(6):429-442 http://www.cell-research.com REVIEW Msx homeobox gene family and craniofacial development SYLVIA ALAPPAT1, ZUN YI ZHANG1, YI PING CHEN1,2* 1Division of Developmental Biology, Department of Cell and Molecular Biology, Tulane University, New orleans, LA 70118, USA. E-mail: [email protected] 2College of Bioengineering, Fujian Normal University, Fuzhou, Fujian Province, China ABSTRACT Vertebrate Msx genes are unlinked, homeobox-containing genes that bear homology to the Drosophila muscle segment homeobox gene. These genes are expressed at multiple sites of tissue-tissue interactions during verte- brate embryonic development. Inductive interactions mediated by the Msx genes are essential for normal craniofacial, limb and ectodermal organ morphogenesis, and are also essential to survival in mice, as manifested by the pheno- typic abnormalities shown in knockout mice and in humans. This review summarizes studies on the expression, regulation, and functional analysis of Msx genes that bear relevance to craniofacial development in humans and mice. Key words: Msx genes, craniofacial, tooth, cleft palate, suture, development, transcription factor, signaling molecule. INTRODUCTION Msx genes have been isolated from a variety of orga- Vertebrate craniofacial organs form from multiple nisms, including ascidians[5, 6], sea urchin[7], zebrafish embryonic tissues including the cranial neural crest [5, 8], frogs[9], birds[10-12], and humans[13]. The mammalian Msx gene family consists of 3 physically derived cells, prechordal mesoderm, and the embryonic unlinked members, named Msx1, Msx2, and Msx3[14, craniofacial ectoderm. Normal craniofacial morphology 15]. Msx3 is only expressed in the dorsal neural tube, in develops as a consequence of complex interactions a pattern resembling that of the prototypical Drosophila between these embryonic tissues, and requires precise msh gene[16, 17]. -
Facets of Mechanical Regulation in the Morphogenesis of Craniofacial Structures
International Journal of Oral Science www.nature.com/ijos REVIEW ARTICLE OPEN FACEts of mechanical regulation in the morphogenesis of craniofacial structures Wei Du1,2, Arshia Bhojwani2 and Jimmy K. Hu 2,3 During embryonic development, organs undergo distinct and programmed morphological changes as they develop into their functional forms. While genetics and biochemical signals are well recognized regulators of morphogenesis, mechanical forces and the physical properties of tissues are now emerging as integral parts of this process as well. These physical factors drive coordinated cell movements and reorganizations, shape and size changes, proliferation and differentiation, as well as gene expression changes, and ultimately sculpt any developing structure by guiding correct cellular architectures and compositions. In this review we focus on several craniofacial structures, including the tooth, the mandible, the palate, and the cranium. We discuss the spatiotemporal regulation of different mechanical cues at both the cellular and tissue scales during craniofacial development and examine how tissue mechanics control various aspects of cell biology and signaling to shape a developing craniofacial organ. International Journal of Oral Science (2021) ;13:4 https://doi.org/10.1038/s41368-020-00110-4 1234567890();,: INTRODUCTION coordinated cell property and behavior changes.3,4 There are four The vertebrate head is an intricate and complex part of the animal main categories of mechanical inputs during development: (1) body, composed of organs with diverse functions and types. These tissue volumetric changes; (2) generation of cellular forces by craniofacial structures, including the cranium, sensory organs, cytoskeletons; (3) large scale forces by muscle contraction; and (4) mandible, temporomandibular joint (TMJ), palate, muscles, and teeth, tissue material properties (Fig.