Pediatric Hydrocele: a Comprehensive Review
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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. -
Cranial Cavitry
Embryology Endo, Energy, and Repro 2017-2018 EMBRYOLOGY OF THE REPRODUCTIVE SYSTEM Janine Prange-Kiel, Ph.D. Office: L1.106, Phone: 83117 Email: [email protected] LEARNING OBJECTIVES: • Name the structures in kidney development that contribute to the development of the reproductive organs. • Predict how the presence or absence of the Y chromosome and the expression of the SRY gene would influence the development of the gonads. • Predict how the presence or absence of testosterone, dihydrotestosterone, and anit- Mullerian hormone would influence the development of the genital ducts and indifferent primordia of the external genitalia. I. Introduction In general, the function of the genital (reproductive) system in males and females is the formation, nurture, and transport of germ cells. In females, an additional function is to provide the proper milieu for the fetal development after conception. Like the urinary system, the genital system derives from intermediate mesoderm. The development of these two systems is tightly interwoven as structures that develop as parts of the urinary system gain function in the genital system. In the adult, the sexual organs differ between males and females. The early genital system, however, is similar in both sexes, and the sexual differentiation of this initially indifferent, bipotential system starts only in the seventh week of embryonic development. The details on how sexual differentiation is determined will be discussed below, but it is worth mentioning here that irregularities in this process result in disorders of sexual differentiation (DSDs). DSDs occur in approximately 1 in 4,500 live births and will be discussed in a separate lecture. -
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. -
ANA214: Systemic Embryology
ANA214: Systemic Embryology ISHOLA, Azeez Olakune [email protected] Anatomy Department, College of Medicine and Health Sciences Outline • Organogenesis foundation • Urogenital system • Respiratory System • Kidney • Larynx • Ureter • Trachea & Bronchi • Urinary bladder • Lungs • Male urethra • Female urethra • Cardiovascular System • Prostate • Heart • Uterus and uterine tubes • Blood vessels • Vagina • Fetal Circulation • External genitalia • Changes in Circulation at Birth • Testes • Gastrointestinal System • Ovary • Mouth • Nervous System • Pharynx • Neurulation • GI Tract • Neural crests • Liver, Spleen, Pancreas Segmentation of Mesoderm • Start by 17th day • Under the influence of notochord • Cells close to midline proliferate – PARAXIAL MESODERM • Lateral cells remain thin – LATERAL PLATE MESODERM • Somatic/Parietal mesoderm – close to amnion • Visceral/Splanchnic mesoderm – close to yolk sac • Intermediate mesoderm connects paraxial and lateral mesoderm Paraxial Mesoderm • Paraxial mesoderm organized into segments – SOMITOMERES • Occurs in craniocaudal sequence and start from occipital region • 1st developed by day 20 (3 pairs per day) – 5th week • Gives axial skeleton Intermediate Mesoderm • Differentiate into Urogenital structures • Pronephros, mesonephros Lateral Plate Mesoderm • Parietal mesoderm + ectoderm = lateral body wall folds • Dermis of skin • Bones + CT of limb + sternum • Visceral Mesoderm + endoderm = wall of gut tube • Parietal mesoderm surrounding cavity = pleura, peritoneal and pericardial cavity • Blood & -
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. -
Genital System
Development of Urogenital System Dr. Ammar Alhaaik Development of Urinary System Diagrams of transverse sections of the embryo - 20 days Intermediate mesoderm Intermediate mesoderm (including adjacent coelom mesothelium) forms a urogenital ridge, consisting of a laterally-positioned nephrogenic cord (that becomes kidneys & ureter) and a medially positioned gonadal ridge (for ovary/testis & female/male genital tract formation). Urinary & genital systems have a common embryonic origin; also, they share common ducts. Nephrogenic cord: develops into three sets of tubular nephric structures (from head to tail :)pronephros mesonephros metanephros) Pronephros— develops during the 4th weekin the cervical region of the intermediate mesoderm . It consists of (7-8) primitive tubules and a pronephric duct that grows caudally and terminates in the cloaca. The tubules soon degenerate, but the pronephric duct persists as the mesonephric duct. Mesonephros: — consists of (70-80) tubules induced to form by the mesonephric duct (former pronephric duct) — one end of each tubule surrounds a glomerulus (vascular proliferation produced by a branch of the dorsal aorta) — the other end of the tubule communicates with the mesonephric duct — eventually, the mesonephros degenerates, but the mesonephric duct becomes epididymis & ductus deferens and some tubules that become incorporated within the testis Metanephros: *becomes adult kidney & ureter of mammals, birds, and reptiles • originates in the pelvic region and moves cranially into the abdomen during embryonic differential growth * lobulated initially but becomes smooth in most species The metanephros originates from two sources: 1- a ureteric bud, which grows out of the mesonephric duct near the cloaca; the bud develops into the ureter, renal pelvis, and numerous collecting ducts; 2- metanephrogenic blastema, which is the caudal region of the nephrogenic cord; the mass forms nephrons NOTE • The pronephros is not functional. -
Yolk Sac Diameter in Multiple Gestations
Case Studies Yolk Sac Diameter in Multiple Gestations Chelsea Fox, MD; Karenne Fru, MD, PhD; and Bruce A. Lessey, MD, PhD From the Department of OB/GYN, Greenville Health System, Greenville, SC (C.F., B.A.L.), University of South Carolina School of Medicine Greenville, Greenville, SC (B.A.L.), and Department of Obstet- rics and Gynecology, New Hanover Regional Medical Center, Wilmington, NC (K.F.) Abstract Enlargement of the yolk sacs is an ominous sign even in multi-gestational pregnancies. he yolk sac functions as the primary route ity conceived after placement of 2 embryos on of exchange between the embryo and post-retrieval day 3. Quantitative hCG levels were Tmother prior to the establishment of the higher than expected and transvaginal ultrasound placental circulation. It is well established that an at 6 weeks’ gestation demonstrated a triplet preg- abnormally large yolk sac serves as a prognostic nancy with a singleton sac and a separate mono- indicator for early pregnancy failure in singleton chorionic-monoamniotic versus conjoined twin gestation. However, no studies have been per- pregnancy with symmetrically enlarged yolk sacs, formed to describe normal versus abnormal yolk each with cardiac activity present (Figs. 1A and B). sac diameters (YSD) in multiple gestations. In this The yolk sacs associated with the twin pregnancy case, we describe a patient with triplet pregnancy were 6.15 mm and 7.37 mm, respectively, while the consisting of monochorionic-monoamniotic singleton had a normal yolk sac. A repeat ultra- twins both with enlarged yolk sacs in addition to sound 10 days later confirmed absence of fetal car- singleton pregnancy in a separate sac with a nor- diac activity in the monochorionic-monoamni- mal yolk sac. -
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. -
Board-Review-Series-Obstetrics-Gynecology-Pearls.Pdf
ObstetricsandGynecology BOARDREVIEW Third Edition Stephen G. Somkuti, MD, PhD Associate Professor Department of Obstetrics and Gynecology and Reproductive Sciences Temple University School of Medicine School Philadelphia, Pennsylvania Director, The Toll Center for Reproductive Sciences Division of Reproductive Endocrinology Department of Obstetrics and Gynecology Abington Memorial Hospital Abington Reproductive Medicine Abington, Pennsylvania New York Chicago San Francisco Lisbon London Madrid Mexico City Milan New Delhi San Juan Seoul Singapore Sydney Toronto Copyright © 2008 by the McGraw-Hill Companies, Inc. All rights reserved. Manufactured in the United States of America. Except as permitted under the United States Copyright Act of 1976, no part of this publication may be reproduced or distributed in any form or by any means, or stored in a database or retrieval system, without the prior written permission of the publisher. 0-07-164298-6 The material in this eBook also appears in the print version of this title: 0-07-149703-X. All trademarks are trademarks of their respective owners. Rather than put a trademark symbol after every occurrence of a trademarked name, we use names in an editorial fashion only, and to the benefit of the trademark owner, with no intention of infringement of the trademark. Where such designations appear in this book, they have been printed with initial caps. McGraw-Hill eBooks are available at special quantity discounts to use as premiums and sales promotions, or for use in corporate training programs. For more information, please contact George Hoare, Special Sales, at [email protected] or (212) 904-4069. TERMS OF USE This is a copyrighted work and The McGraw-Hill Companies, Inc. -
Mesonephric Duct, a Continuation of the Pronephric Duct
Anhui Medical University Development of the Urogenital System Lyu Zhengmei Department of Histology and Embryology Anhui Medical University Anhui Medical University ORIGINS----mesoderm ---paraxial mesoderm: somite ---intermediate mesoderm urinary and genital system ---lateral mesoderm paraxial neural intermediate mesoderm groove mesoderm endoderm notochord lateral mesoderm Anhui Medical University Part I Introduction The 【】※ origins of origins of urogenital urogenital system system?? Anhui Medical University differentiation of intermediate mesoderm •intermediate mesoderm Nephrotome nephrogenic cord urogenital ridge mesonephric ridge,gonadal ridge Anhui Medical University 1.Formation of nephrotome Nephrotome: The cephalic portion of intermediate mesoderm becomes segmented, which forms pronephric system and degenerates early. 4 weeks Anhui Medical University intermediate 2.Nephrogenic cord mesoderm Its caudal part gradually isolated from somites, forming two longitudinal elevation along the posterior wall of abdominal cavity Nephrogenic cord urogenital ridge Anhui Medical University 3. Urogenital ridge Mesonephric ridge: The outside part of the urogenital ridge giving rise to the urinary system Gonadal ridge: the innerside part giving rise to the genital system Anhui Medical University Part II Development of Urinary system Three sets of kidney occur in embryo developmnet ( 1)pronephros (2) mesonephros (3) metanephros Development of Bladder and urethra Cloaca Urogenital sinus Congenital anomalies of the urinary system Anhui Medical University -
1- Development of Female Genital System
Development of female genital systems Reproductive block …………………………………………………………………. Objectives : ✓ Describe the development of gonads (indifferent& different stages) ✓ Describe the development of the female gonad (ovary). ✓ Describe the development of the internal genital organs (uterine tubes, uterus & vagina). ✓ Describe the development of the external genitalia. ✓ List the main congenital anomalies. Resources : ✓ 435 embryology (males & females) lectures. ✓ BRS embryology Book. ✓ The Developing Human Clinically Oriented Embryology book. Color Index: ✓ EXTRA ✓ Important ✓ Day, Week, Month Team leaders : Afnan AlMalki & Helmi M AlSwerki. Helpful video Focus on female genital system INTRODUCTION Sex Determination - Chromosomal and genetic sex is established at fertilization and depends upon the presence of Y or X chromosome of the sperm. - Development of female phenotype requires two X chromosomes. - The type of sex chromosomes complex established at fertilization determine the type of gonad differentiated from the indifferent gonad - The Y chromosome has testis determining factor (TDF) testis determining factor. One of the important result of fertilization is sex determination. - The primary female sexual differentiation is determined by the presence of the X chromosome , and the absence of Y chromosome and does not depend on hormonal effect. - The type of gonad determines the type of sexual differentiation in the Sexual Ducts and External Genitalia. - The Female reproductive system development comprises of : Gonad (Ovary) , Genital Ducts ( Both male and female embryo have two pair of genital ducts , They do not depend on ovaries or hormones ) and External genitalia. DEVELOPMENT OF THE GONADS (ovaries) - Is Derived From Three Sources (Male Slides) 1. Mesothelium 2. Mesenchyme 3. Primordial Germ cells (mesodermal epithelium ) lining underlying embryonic appear among the Endodermal the posterior abdominal wall connective tissue cell s in the wall of the yolk sac).