Yolk Sac Diameter in Multiple Gestations
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3 Embryology and Development
BIOL 6505 − INTRODUCTION TO FETAL MEDICINE 3. EMBRYOLOGY AND DEVELOPMENT Arlet G. Kurkchubasche, M.D. INTRODUCTION Embryology – the field of study that pertains to the developing organism/human Basic embryology –usually taught in the chronologic sequence of events. These events are the basis for understanding the congenital anomalies that we encounter in the fetus, and help explain the relationships to other organ system concerns. Below is a synopsis of some of the critical steps in embryogenesis from the anatomic rather than molecular basis. These concepts will be more intuitive and evident in conjunction with diagrams and animated sequences. This text is a synopsis of material provided in Langman’s Medical Embryology, 9th ed. First week – ovulation to fertilization to implantation Fertilization restores 1) the diploid number of chromosomes, 2) determines the chromosomal sex and 3) initiates cleavage. Cleavage of the fertilized ovum results in mitotic divisions generating blastomeres that form a 16-cell morula. The dense morula develops a central cavity and now forms the blastocyst, which restructures into 2 components. The inner cell mass forms the embryoblast and outer cell mass the trophoblast. Consequences for fetal management: Variances in cleavage, i.e. splitting of the zygote at various stages/locations - leads to monozygotic twinning with various relationships of the fetal membranes. Cleavage at later weeks will lead to conjoined twinning. Second week: the week of twos – marked by bilaminar germ disc formation. Commences with blastocyst partially embedded in endometrial stroma Trophoblast forms – 1) cytotrophoblast – mitotic cells that coalesce to form 2) syncytiotrophoblast – erodes into maternal tissues, forms lacunae which are critical to development of the uteroplacental circulation. -
The Derivatives of Three-Layered Embryo (Germ Layers)
HUMANHUMAN EMBRYOLOGYEMBRYOLOGY Department of Histology and Embryology Jilin University ChapterChapter 22 GeneralGeneral EmbryologyEmbryology FourthFourth week:week: TheThe derivativesderivatives ofof trilaminartrilaminar germgerm discdisc Dorsal side of the germ disc. At the beginning of the third week of development, the ectodermal germ layer has the shape of a disc that is broader in the cephalic than the caudal region. Cross section shows formation of trilaminar germ disc Primitive pit Drawing of a sagittal section through a 17-day embryo. The most cranial portion of the definitive notochord has formed. ectoderm Schematic view showing the definitive notochord. horizon =ectoderm hillside fields =neural plate mountain peaks =neural folds Cave sinks into mountain =neural tube valley =neural groove 7.1 Derivatives of the Ectodermal Germ Layer 1) Formation of neural tube Notochord induces the overlying ectoderm to thicken and form the neural plate. Cross section Animation of formation of neural plate When notochord is forming, primitive streak is shorten. At meanwhile, neural plate is induced to form cephalic to caudal end, following formation of notochord. By the end of 3rd week, neural folds and neural groove are formed. Neural folds fuse in the midline, beginning in cervical region and Cross section proceeding cranially and caudally. Neural tube is formed & invade into the embryo body. A. Dorsal view of a human embryo at approximately day 22. B. Dorsal view of a human embryo at approximately day 23. The nervous system is in connection with the amniotic cavity through the cranial and caudal neuropores. Cranial/anterior neuropore Neural fold heart Neural groove endoderm caudal/posterior neuropore A. -
What Is the Role of the Placenta—Does It Protect Against Or Is It a Target for Insult?
Teratology Primer, 3rd Edition www.teratology.org/primer What Is the Role of the Placenta—Does It Protect Against or Is It a Target for Insult? Richard K. Miller University of Rochester School of Medicine & Dentistry Rochester, New York The placenta is not just a barrier but has many functions that are vital to the health of the embryo/fetus. The placenta is the anchor, the conduit, and the controller of pregnancy—and it can also be a target for toxicant action. The placenta encompasses not only the chorioallantoic placenta but all of its extraembryonic membranes (chorion/amnion) and the yolk sac. (Figure 1). The placenta and its membranes secure the embryo and fetus to the decidua (uterine lining) and release a variety of steroid and protein hormones that characterize the physiology of the pregnant female. Figure 1. Placental Structure in the Mouse. Figures depict early development of the mouse conceptus at embryonic days (E3.5, E7.5, E12.5). In the fetus, the visceral yolk sac (vYS) inverts and remains active throughout the entire gestation providing for transfer of selective large molecules, e.g., immunoglobulins IgG and vitamin B12. Abbreviations: Al, allantois; Am, amnion; Ch, chorion; Dec, decidua; Emb, embryo; Epc, ectoplacental cone; ICM, inner cell mass; Lab, Labyrinth; pYS, parietal yolk sac; SpT, spongiotrophoblast; TCG, trophoblast giant cell; Umb Cord, umbilical cord; vYS, visceral yolk sac; C-TGC, maternal blood canal trophoblast giant cell; P-TGC, parietal trophoblast giant cell; S-TGC, sinusoidal trophoblast giant cell; SpA-TGC, Spiral artery-associated trophoblast giant cell; Cyan-trophectoderm and trophoblast lineage, Black- inner cell mass and embryonic ectoderm; Gray -endoderm, Red-maternal vasculature, Purple-mesoderm, Yellow- decidua, Pink-fetal blood vessels in labyrinth. -
Human Embryologyembryology
HUMANHUMAN EMBRYOLOGYEMBRYOLOGY Department of Histology and Embryology Jilin University ChapterChapter 22 GeneralGeneral EmbryologyEmbryology DevelopmentDevelopment inin FetalFetal PeriodPeriod 8.1 Characteristics of Fetal Period 210 days, from week 9 to delivery. characteristics: maturation of tissues and organs rapid growth of the body During 3-5 month, fetal growth in length is 5cm/M. In last 2 month, weight increases in 700g/M. relative slowdown in growth of the head compared with the rest of the body 8.2 Fetal AGE Fertilization age lasts 266 days, from the moment of fertilization to the day when the fetal is delivered. menstrual age last 280 days, from the first day of the last menstruation before pregnancy to the day when the fetal is delivered. The formula of expected date of delivery: year +1, month -3, day+7. ChapterChapter 22 GeneralGeneral EmbryologyEmbryology FetalFetal membranesmembranes andand placentaplacenta Villous chorion placenta Decidua basalis Umbilical cord Afterbirth/ secundines Fusion of amnion, smooth chorion, Fetal decidua capsularis, membrane decidua parietalis 9.1 Fetal Membranes TheThe fetalfetal membranemembrane includesincludes chorionchorion,, amnion,amnion, yolkyolk sac,sac, allantoisallantois andand umbilicalumbilical cord,cord, originatingoriginating fromfrom blastula.blastula. TheyThey havehave functionsfunctions ofof protection,protection, nutrition,nutrition, respiration,respiration, excretion,excretion, andand producingproducing hormonehormone toto maintainmaintain thethe pregnancy.pregnancy. delivery 1) Chorion: villous and smooth chorion Villus chorionic plate primary villus trophoblast secondary villus extraembryonic tertiary villus mesoderm stem villus Amnion free villus decidua parietalis Free/termin al villus Stem/ancho chorion ring villus Villous chorion Smooth chorion Amniotic cavity Extraembyonic cavity disappears gradually; Amnion is added into chorionic plate; Villous and smooth chorion is formed. -
Embryology and Teratology in the Curricula of Healthcare Courses
ANATOMICAL EDUCATION Eur. J. Anat. 21 (1): 77-91 (2017) Embryology and Teratology in the Curricula of Healthcare Courses Bernard J. Moxham 1, Hana Brichova 2, Elpida Emmanouil-Nikoloussi 3, Andy R.M. Chirculescu 4 1Cardiff School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, Wales, United Kingdom and Department of Anatomy, St. George’s University, St George, Grenada, 2First Faculty of Medicine, Institute of Histology and Embryology, Charles University Prague, Albertov 4, 128 01 Prague 2, Czech Republic and Second Medical Facul- ty, Institute of Histology and Embryology, Charles University Prague, V Úvalu 84, 150 00 Prague 5 , Czech Republic, 3The School of Medicine, European University Cyprus, 6 Diogenous str, 2404 Engomi, P.O.Box 22006, 1516 Nicosia, Cyprus , 4Department of Morphological Sciences, Division of Anatomy, Faculty of Medicine, C. Davila University, Bucharest, Romania SUMMARY Key words: Anatomy – Embryology – Education – Syllabus – Medical – Dental – Healthcare Significant changes are occurring worldwide in courses for healthcare studies, including medicine INTRODUCTION and dentistry. Critical evaluation of the place, tim- ing, and content of components that can be collec- Embryology is a sub-discipline of developmental tively grouped as the anatomical sciences has biology that relates to life before birth. Teratology however yet to be adequately undertaken. Surveys (τέρατος (teratos) meaning ‘monster’ or ‘marvel’) of teaching hours for embryology in US and UK relates to abnormal development and congenital medical courses clearly demonstrate that a dra- abnormalities (i.e. morphofunctional impairments). matic decline in the importance of the subject is in Embryological studies are concerned essentially progress, in terms of both a decrease in the num- with the laws and mechanisms associated with ber of hours allocated within the medical course normal development (ontogenesis) from the stage and in relation to changes in pedagogic methodol- of the ovum until parturition and the end of intra- ogies. -
Organogenesis Part 2 ______
Organogenesis Part 2 ___________________________________ ___________________________________ V. Lateral Plate Mesoderm VI. Endoderm ___________________________________ VII. Development of the Tetrapod Limb VIII. Sex Determination ___________________________________ ___________________________________ ___________________________________ ___________________________________ V. Lateral Plate Mesoderm ___________________________________ ___________________________________ paraxial mesoderm chordamesoderm intermediate mesoderm ___________________________________ ___________________________________ ___________________________________ lateral plate mesoderm ___________________________________ ___________________________________ Lateral Plate Mesoderm ___________________________________ Terminology: - Somatopleure: somatic mesoderm plus ectoderm ___________________________________ - Splanchnopleure: splanchnic mesoderm plus endoderm - Coelom: body cavity forms between them ___________________________________ ___________________________________ ___________________________________ ___________________________________ ___________________________________ Lateral Plate Mesoderm ___________________________________ • The Coelom: ___________________________________ – eventually left and right cavities fuse into one ___________________________________ – runs from neck to anus in vertebrates – portioned off by folds of somatic mesoderm ___________________________________ • pleural cavity: surrounds the thorax and lungs • pericardial cavity: surrounds the -
Unit 3 Embryo Questions
Unit 3 Embryology Clinically Oriented Anatomy (COA) Texas Tech University Health Sciences Center Created by Parker McCabe, Fall 2019 parker.mccabe@@uhsc.edu Solu%ons 1. B 11. A 21. D 2. C 12. B 22. D 3. C 13. E 23. D 4. B 14. D 24. A 5. E 15. C 25. D 6. C 16. B 26. B 7. D 17. E 27. C 8. B 18. A 9. C 19. C 10. D 20. B Digestive System 1. Which of the following structures develops as an outgrowth of the endodermal epithelium of the upper part of the duodenum? A. Stomach B. Pancreas C. Lung buds D. Trachea E. Esophagus Ques%on 1 A. Stomach- Foregut endoderm B. Pancreas- The pancreas, liver, and biliary apparatus all develop from outgrowths of the endodermal epithelium of the upper part of the duodenum. C. Lung buds- Foregut endoderm D. Trachea- Foregut endoderm E. Esophagus- Foregut endoderm 2. Where does the spleen originate and then end up after the rotation of abdominal organs during fetal development? A. Ventral mesentery à left side B. Ventral mesentery à right side C. Dorsal mesentery à left side D. Dorsal mesentery à right side E. It does not relocate Question 2 A. Ventral mesentery à left side B. Ventral mesentery à right side C. Dorsal mesentery à left side- The spleen and dorsal pancreas are embedded within the dorsal mesentery (greater omentum). After rotation, dorsal will go to the left side of the body and ventral will go to the right side of the body (except for the ventral pancreas). -
Ultrasound in the First Trimester
ULTRASOUND IN THE 4 FIRST TRIMESTER INTRODUCTION First trimester ultrasound is often done to assess pregnancy location and thus it overlaps between an obstetric and gynecologic ultrasound examination. Accurate performance of an ultrasound examination in the first trimester is important given its ability to confirm an intrauterine gestation, assess viability and number of embryo(s) and accurately date a pregnancy, all of which are critical for the course of pregnancy. Main objectives of the first trimester ultrasound examination are listed in Table 4.1. These objectives may differ somewhat based upon the gestational age within the first trimester window, be it 6 weeks, 9 weeks, or 12 weeks, but the main goals are identical. In this chapter, the approach to the first trimester ultrasound examination will be first discussed followed by the indications to the ultrasound examination in early gestation. Chronologic sequence of the landmarks of the first trimester ultrasound in the normal pregnancy will be described and ultrasound findings of pregnancy failure will be presented. The chapter will also display some of the major fetal anomalies that can be recognized by ultrasound in the first trimester. Furthermore, given the importance of first trimester assignment of chorionicity in multiple pregnancies, this topic will also be addressed in this chapter. TABLE 4.1 Main Objectives of Ultrasound Examination in the First Trimester - Confirmation of pregnancy - Intrauterine localization of gestational sac - Confirmation of viability (cardiac activity in embryo/fetus) - Detection of signs of early pregnancy failure - Single vs. Multiple pregnancy (define chorionicity in multiples) - Assessment of gestational age (pregnancy dating) - Assessment of normal embryo and gestational sac before 10 weeks - Assessment of basic anatomy after 11 week TRANSVAGINAL ULTRASOUND EXAMINATION IN THE FIRST TRIMESTER There is general consensus that, with rare exceptions, ultrasound examination in the first trimester of pregnancy should be performed transvaginally. -
First, Do No Harm . . . to Early Pregnancies
295jum_online.qxp:Layout 1 4/25/10 3:04 PM Page 685 Editorial First, Do No Harm . to Early Pregnancies Peter M. Doubilet, MD, PhD Carol B. Benson, MD Department of Radiology Brigham and Women’s Hospital Harvard Medical School Boston, Massachusetts USA hen a woman of childbearing age presents to a physician or other care- giver complaining of vaginal bleeding and/or pelvic pain, a pelvic ultra- sound examination is often performed to assess the etiology of her symptoms.1,2 If she has a positive pregnancy test, the major role of ultra- Wsound is to assess whether she has a normal intrauterine pregnancy (IUP), an abnor- mal IUP, or an ectopic pregnancy. The information provided by ultrasound can be of great value in guiding management decisions and improving outcome. Errors in ultrasound interpretation, however, can lead to mismanagement and, there- by, to bad pregnancy outcome. Potential interpretation errors include: (1) failure to conclude that there is a definite or probable IUP despite ultrasound images depicting such a finding; and (2) failure to conclude that there is a definite or probable ectopic pregnancy despite ultrasound images depicting such a finding. This editorial focuses on the former error. Definition and Scope of the Problem The issue addressed here involves the situation in which a woman with a positive preg- nancy test and symptoms of bleeding and/or pain undergoes a pelvic ultrasound examination, and the scan demonstrates a nonspecific intrauterine fluid collection (Figure 1). By “nonspecific,” we mean a fluid collection with curved edges in the central echogenic portion of the uterus (ie, in the decidua) with no visible embryo or yolk sac, that does not demonstrate one of the published signs of early IUP (double sac sign3 or intradecidual sign4). -
Development of the Genital System Development of the Gonads
Development of the Genital System Development of the gonads Dr Ahmed Salman The gonads develop form three sources (the first two are mesodermal, the third one is endodermal ) . 1.Proliferating coelomic epithelium on the medial side of the mesonephros. 2. Adjacent mesenchyme dorsal to the proliferating coelomic epithelium. 3. Primordial germ cells (endodermal), which develop in the wall of the yolk sac and migrate along the dorsal mesentery to reach the developing gonad. DR AHMED SALMAN The indifferent stage of the developing gonads - The coelomic epithelium (on either side of the aorta) proliferates and becomes multi layered and forms a longitudinal projection into the coelomic cavity called the genital ridge. - The genital ridge forms a number of epithelial cords called the primary sex cords that invade the underlying mesenchyme, which separate the cords from each other. - Up to the 6th or 7th week, the developing gonad cannot be differentiated into testis or ovary. DR AHMED SALMAN DR AHMED SALMAN Development of the testis and its descent Under the effect of the testis determining factor (T.D.F) present on the short arm of Y - chromosome, the undifferentiated gonad is switched to form a testis. 1. The coelomic epithelium. - The primary sex cords elongate to form testis cords (future seminiferous tubules) which undergo three important events : • Ventrally, they lose contact with the surface epithelium by the developing tunica albuginae. • Dorsally, they communicate with each other to form rete testis. • Internally, they are invaded by the primitive germ cells. DR AHMED SALMAN The testis cords become lined by two types of cells: A. -
26 April 2010 TE Prepublication Page 1 Nomina Generalia General Terms
26 April 2010 TE PrePublication Page 1 Nomina generalia General terms E1.0.0.0.0.0.1 Modus reproductionis Reproductive mode E1.0.0.0.0.0.2 Reproductio sexualis Sexual reproduction E1.0.0.0.0.0.3 Viviparitas Viviparity E1.0.0.0.0.0.4 Heterogamia Heterogamy E1.0.0.0.0.0.5 Endogamia Endogamy E1.0.0.0.0.0.6 Sequentia reproductionis Reproductive sequence E1.0.0.0.0.0.7 Ovulatio Ovulation E1.0.0.0.0.0.8 Erectio Erection E1.0.0.0.0.0.9 Coitus Coitus; Sexual intercourse E1.0.0.0.0.0.10 Ejaculatio1 Ejaculation E1.0.0.0.0.0.11 Emissio Emission E1.0.0.0.0.0.12 Ejaculatio vera Ejaculation proper E1.0.0.0.0.0.13 Semen Semen; Ejaculate E1.0.0.0.0.0.14 Inseminatio Insemination E1.0.0.0.0.0.15 Fertilisatio Fertilization E1.0.0.0.0.0.16 Fecundatio Fecundation; Impregnation E1.0.0.0.0.0.17 Superfecundatio Superfecundation E1.0.0.0.0.0.18 Superimpregnatio Superimpregnation E1.0.0.0.0.0.19 Superfetatio Superfetation E1.0.0.0.0.0.20 Ontogenesis Ontogeny E1.0.0.0.0.0.21 Ontogenesis praenatalis Prenatal ontogeny E1.0.0.0.0.0.22 Tempus praenatale; Tempus gestationis Prenatal period; Gestation period E1.0.0.0.0.0.23 Vita praenatalis Prenatal life E1.0.0.0.0.0.24 Vita intrauterina Intra-uterine life E1.0.0.0.0.0.25 Embryogenesis2 Embryogenesis; Embryogeny E1.0.0.0.0.0.26 Fetogenesis3 Fetogenesis E1.0.0.0.0.0.27 Tempus natale Birth period E1.0.0.0.0.0.28 Ontogenesis postnatalis Postnatal ontogeny E1.0.0.0.0.0.29 Vita postnatalis Postnatal life E1.0.1.0.0.0.1 Mensurae embryonicae et fetales4 Embryonic and fetal measurements E1.0.1.0.0.0.2 Aetas a fecundatione5 Fertilization -
RNA-Seq Reveals Conservation of Function Among the Yolk Sacs Of
RNA-seq reveals conservation of function among the PNAS PLUS yolk sacs of human, mouse, and chicken Tereza Cindrova-Daviesa, Eric Jauniauxb, Michael G. Elliota,c, Sungsam Gongd,e, Graham J. Burtona,1, and D. Stephen Charnock-Jonesa,d,e,1,2 aCentre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, CB2 3EG, United Kingdom; bElizabeth Garret Anderson Institute for Women’s Health, Faculty of Population Health Sciences, University College London, London, WC1E 6BT, United Kingdom; cSt. John’s College, University of Cambridge, Cambridge, CB2 1TP, United Kingdom; dDepartment of Obstetrics and Gynaecology, University of Cambridge, Cambridge, CB2 0SW, United Kingdom; and eNational Institute for Health Research, Cambridge Comprehensive Biomedical Research Centre, Cambridge, CB2 0QQ, United Kingdom Edited by R. Michael Roberts, University of Missouri-Columbia, Columbia, MO, and approved May 5, 2017 (received for review February 14, 2017) The yolk sac is phylogenetically the oldest of the extraembryonic yolk sac plays a critical role during organogenesis (3–5, 8–10), membranes. The human embryo retains a yolk sac, which goes there are limited data to support this claim. Obtaining experi- through primary and secondary phases of development, but its mental data for the human is impossible for ethical reasons, and importance is controversial. Although it is known to synthesize thus we adopted an alternative strategy. Here, we report RNA proteins, its transport functions are widely considered vestigial. sequencing (RNA-seq) data derived from human and murine yolk Here, we report RNA-sequencing (RNA-seq) data for the human sacs and compare them with published data from the yolk sac of and murine yolk sacs and compare those data with data for the the chicken.