Ultrasound in the First Trimester
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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. -
Management of Patent Vitellointestinal Duct in Infants
Published online: 2021-02-17 94 OriginalPatent Vitellointestinal Article Duct Ghritlaharey Management of Patent Vitellointestinal Duct in Infants Rajendra K. Ghritlaharey1 1Department of Paediatric Surgery, Gandhi Medical College and Address for correspondence Rajendra K. Ghritlaharey, MS, MCh, Associated Kamla Nehru and Hamidia Hospital, Bhopal, Madhya FAIS, MAMS, DLitt, Department of Paediatric Surgery, Gandhi Medical Pradesh, India College and Associated Kamla Nehru and Hamidia Hospitals, Bhopal 462001, Madhya Pradesh, India (e-mail: [email protected]). Ann Natl Acad Med Sci (India) 2021;57:94–99. Abstract Objectives This study was undertaken to investigate and review the clinical presen- tation, surgical procedures executed, and the final outcome of infants managed for the patent vitellointestinal duct. Materials and Methods This is a single-institution, retrospective study and included infants who were operated for the patent vitellointestinal duct. This study was conducted at author’s Department of Paediatric Surgery during the last 20 years; from January 1, 2000 to December 31, 2019. Results A total of 24 infants were operated for the patent vitellointestinal duct during the study period and comprised 20 (83.3%) boys and 4 (16.6%) girls. The age of infants ranged from 7 days to 10 months, with a mean of 88.41 ± 64.9 days. Twenty-three (95.8%) infants were operated within 6 months of the age, 17 (70.8%) of them were operated within 3 months of the age. Only one (4.1%) infant was operated at the age of 10 months. Among 24 infants, 13 (54.1%) were presented with features suggestive of acute intestinal obstruction and remaining 11 (45.8%) were presented with fecal discharges through the umbilicus without intestinal obstruction. -
PRG2 and AQPEP Are Misexpressed in Fetal Membranes in Placenta Previa and Percreta Elisa T. Zhang1, Roberta L. Hannibal1,6, Keyl
bioRxiv preprint doi: https://doi.org/10.1101/2020.08.14.248807; this version posted August 14, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. 1 PRG2 and AQPEP are misexpressed in fetal membranes in placenta previa and percreta 2 3 Elisa T. Zhang1, Roberta L. Hannibal1,6, Keyla M. Badillo Rivera1,7, Janet H.T. Song1,8, Kelly 4 McGowan1, Xiaowei Zhu1,2, Gudrun Meinhardt3, Martin Knöfler3, Jürgen Pollheimer3, Alexander 5 E. Urban1,2, Ann K. Folkins4, Deirdre J. Lyell5, Julie C. Baker1,5* 6 7 1DepartMent of Genetics, Stanford University School of Medicine, Stanford, California, United 8 States of AMerica. 9 2DepartMent of Psychiatry and Behavioral Sciences, Stanford University School of 10 Medicine, Stanford, California, United States of AMerica. 11 3DepartMent of Obstetrics and Gynaecology, Reproductive Biology Unit, Medical University of 12 Vienna, Vienna, Austria. 13 4DepartMent of Pathology, Stanford University School of Medicine, Stanford, California, United 14 States of AMerica. 15 5DepartMent of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, 16 California, United States of AMerica. 17 6Present address: Second GenoMe, Inc., Brisbane, California, United States of AMerica. 18 7Present address: Eversana Consulting, South San Francisco, California, United States of 19 AMerica. 20 8Present address: Division of Genetics and GenoMics, Boston Children’s Hospital, Harvard 21 Medical School, Boston, Massachusetts, United States of AMerica. 22 23 *Correspondence: [email protected] 24 300 Pasteur Dr. -
Extremely Rare Presentation of an Omphalomesenteric Cyst in a 61-Year-Old Patient
Turk J Surg 2017; 33: 43-44 Case Report DOI: 10.5152/UCD.2014.2748 Extremely rare presentation of an omphalomesenteric cyst in a 61-year-old patient Recep Aktimur1, Uğur Yaşar2, Elif Çolak1, Nuraydın Özlem1 ABSTRACT The umbilicus is remaining scar tissue from the umbilical cord in the fetus. If the omphalomesenteric duct in the umbilicus is not properly closed, an ileal-umbilical fistula, sinus formation, cysts, or, most commonly, Meckel’s di- verticulum can develop. The others are very rare and mostly occur in the pediatric population. We describe herein a 61-year-old female with a giant omphalomesenteric cyst presented as an asymptomatic infraumbilical mass. To our knowledge, this is the oldest patient reported and the largest cyst described in the literature. The diagnosis of a painless abdominal mass frequently suggests malignancy in older patients. But, extremely rare conditions can be detected, such as an omphalomesenteric cyst. Keywords: Adult, anomaly, cyst, duct, omphalomesenteric INTRODUCTION The umbilicus is remaining scar tissue from the umbilical cord in the fetus. It contains the urachus, om- phalomesenteric duct, and the round ligament’s embryonic remnants, which can be a source of many clinical problems. Also, umbilical hernia can occur in cases of closure defects of the umbilical ring. If the omphalomesenteric duct is not properly closed, an ileal-umbilical fistula, sinus formation, cysts, or Meckel’s diverticulum can develop. Meckel’s diverticulum is the most common omphalomesenteric duct anomaly, and it is also the most common congenital abnormality of the gastrointestinal tract (2%). Other anomalies associated with the omphalomesenteric duct are very rare and mostly occur in the pediatric population. -
Massive Subchorionic Haemorrhage: a Rare Case Report Associated with Secondary PPH Due to Uterine Artery Pseudoaneurysm
International Journal of Reproduction, Contraception, Obstetrics and Gynecology Arumaikannu J et al. Int J Reprod Contracept Obstet Gynecol. 2017 Oct;6(10):4723-4726 www.ijrcog.org pISSN 2320-1770 | eISSN 2320-1789 DOI: http://dx.doi.org/10.18203/2320-1770.ijrcog20174475 Case Report Massive subchorionic haemorrhage: a rare case report associated with secondary PPH due to uterine artery pseudoaneurysm J. Arumaikannu*, S. Usha Rani, T. S. Aarifa Thasleem Institute of Obstetrics and Gynecology, Egmore, Chennai, Tamil Nadu, India Received: 08 August 2017 Accepted: 04 September 2017 *Correspondence: Dr. J. Arumaikannu, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Massive subchorionic hemorrhage is a rare but serious condition in pregnancy in which a large amount of blood, mainly maternal collects between the uterine wall and the chorionic membrane and may leak through the cervical canal. Although many associations have been reported, an underlying etiology has not been elucidated. Association of massive subchorionic hemorrhage with thrombophilias have been reported in few articles. We are reporting a case of massive subchorionic hemorrhage presented at 13 weeks of gestation associated with secondary post-partum hemorrhage due to uterine artery pseudoaneurysm. Keywords: Massive subchorionic haemorrhage, Secondary PPH, Uterine artery pseudoaneurysm INTRODUCTION hemorrhage in the second trimester may also compromise maternal health.2,3 During pregnancy, minor degrees of haemorrhage on the chorionic plate surface of the placenta are commonly A subchorionic hemorrhage can be considered large or identified on ultrasound assessment. -
Self-Organized Amniogenesis by Human Pluripotent Stem Cells in a Biomimetic Implantation-Like Niche
LETTERS PUBLISHED ONLINE: 12 DECEMBER 2016 | DOI: 10.1038/NMAT4829 Self-organized amniogenesis by human pluripotent stem cells in a biomimetic implantation-like niche Yue Shao1†, Kenichiro Taniguchi2†, Katherine Gurdziel3, Ryan F. Townshend2, Xufeng Xue1, Koh Meng Aw Yong1, Jianming Sang1, Jason R. Spence2, Deborah L. Gumucio2* and Jianping Fu1,2,4* Amniogenesis—the development of amnion—is a critical factors seen in the in vivo amniogenic niche: a three-dimensional developmental milestone for early human embryogenesis (3D) extracellular matrix (ECM) that is provided by the basement and successful pregnancy1,2. However, human amniogenesis membrane surrounding the epiblast during implantation11; and a is poorly understood due to limited accessibility to peri- soft tissue bed provided by the uterine wall and trophoblast to implantation embryos and a lack of in vitro models. Here support the developing amnion (Fig. 1a,b). Since amniogenesis ini- we report an ecient biomaterial system to generate human tiates from the expanding pluripotent epiblast, we utilized mTeSR1 amnion-like tissue in vitro through self-organized development medium and basement membrane matrix (Geltrex) to render the of human pluripotent stem cells (hPSCs) in a bioengineered culture permissive for pluripotency maintenance. niche mimicking the in vivo implantation environment. We In this culture system, H9 human embryonic stem cells (hESCs) show that biophysical niche factors act as a switch to toggle were plated as single cells at 30,000 cells cm−2 onto a thick, hPSC self-renewal versus amniogenesis under self-renewal- soft gel bed of Geltrex (with thickness ≥100 µm, bulk Young's permissive biochemical conditions. We identify a unique modulus ∼900 Pa, coated on a glass coverslip), in mTeSR1 medium molecular signature of hPSC-derived amnion-like cells and supplemented with the ROCK inhibitor Y27632 (Fig. -
A Guide to Obstetrical Coding Production of This Document Is Made Possible by Financial Contributions from Health Canada and Provincial and Territorial Governments
ICD-10-CA | CCI A Guide to Obstetrical Coding Production of this document is made possible by financial contributions from Health Canada and provincial and territorial governments. The views expressed herein do not necessarily represent the views of Health Canada or any provincial or territorial government. Unless otherwise indicated, this product uses data provided by Canada’s provinces and territories. All rights reserved. The contents of this publication may be reproduced unaltered, in whole or in part and by any means, solely for non-commercial purposes, provided that the Canadian Institute for Health Information is properly and fully acknowledged as the copyright owner. Any reproduction or use of this publication or its contents for any commercial purpose requires the prior written authorization of the Canadian Institute for Health Information. Reproduction or use that suggests endorsement by, or affiliation with, the Canadian Institute for Health Information is prohibited. For permission or information, please contact CIHI: Canadian Institute for Health Information 495 Richmond Road, Suite 600 Ottawa, Ontario K2A 4H6 Phone: 613-241-7860 Fax: 613-241-8120 www.cihi.ca [email protected] © 2018 Canadian Institute for Health Information Cette publication est aussi disponible en français sous le titre Guide de codification des données en obstétrique. Table of contents About CIHI ................................................................................................................................. 6 Chapter 1: Introduction .............................................................................................................. -
Drug Use and Pregnancy
Rochester Institute of Technology RIT Scholar Works Theses 7-28-1999 Drug use and pregnancy Kimberly Klapmust Follow this and additional works at: https://scholarworks.rit.edu/theses Recommended Citation Klapmust, Kimberly, "Drug use and pregnancy" (1999). Thesis. Rochester Institute of Technology. Accessed from This Thesis is brought to you for free and open access by RIT Scholar Works. It has been accepted for inclusion in Theses by an authorized administrator of RIT Scholar Works. For more information, please contact [email protected]. ROCHESTER INSTITUTE OF TECHNOLOGY A Thesis Submitted to the Faculty of The College of Imaging Arts and Sciences In Candidacy for the Degree of MASTER OF FINE ARTS Drug Use and Pregnancy by Kimberly A. Klapmust July 28, 1999 Approvals Adviser: Robert Wabnitz Date: Associate Adviser. Dr. Nancy Wanek ~)14 Date: \\.\,, c Associate Advisor: Glen Hintz Date ]I-I, zJ Cf9 I 7 Department ChaiIWrson: _ Dale: 1//17._/c; '1 I, , hereby deny permission to the Wallace Memorial library of RIT to reproduce my thesis in whole or in part. Any reproduction will not be for commercial use or profit. INTRODUCTION Human development is a remarkably complex process whereby the union of two small cells can after a period of time give rise to a new human being, complete with vital organs, bones, muscles, nerves, blood vessels, and much more. Considering the intricacy of the developmental process, it is indeed miraculous that most babies are born healthy. Some children, however, are born with abnormalities. Environmental agents, such as drugs, are responsible for some of these abnormalities. -
BMP-Treated Human Embryonic Stem Cells Transcriptionally Resemble Amnion Cells in the Monkey Embryo
bioRxiv preprint doi: https://doi.org/10.1101/2021.01.21.427650; this version posted January 22, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. BMP-treated human embryonic stem cells transcriptionally resemble amnion cells in the monkey embryo Sapna Chhabra1,2,3, Aryeh Warmflash2,4* 1Systems Synthetic and Physical Biology graduate program, 2Department of Biosciences, 4Department of Bioengineering, Rice University, Houston, TX 77005 3Present address: Developmental Biology Unit, EMBL Heidelberg. *Correspondence to AW: [email protected] Abstract Human embryonic stem cells (hESCs) possess an immense potential to generate clinically relevant cell types and unveil mechanisms underlying early human development. However, using hESCs for discovery or translation requires accurately identifying differentiated cell types through comparison with their in vivo counterparts. Here, we set out to determine the identity of much debated BMP-treated hESCs by comparing their transcriptome to the recently published single cell transcriptomes of early human embryos in the study Xiang et al 2019. Our analyses reveal several discrepancies in the published human embryo dataset, including misclassification of putative amnion, intermediate and inner cell mass cells. These misclassifications primarily resulted from similarities in pseudogene expression, highlighting the need to carefully consider gene lists when making comparisons between cell types. In the absence of a relevant human dataset, we utilized the recently published single cell transcriptome of the early post implantation monkey embryo to discern the identity of BMP-treated hESCs. -
Folding of Embryo
❑There is progressive increase in the size of the embryonic disc due to rapid growth of cells of central part of embryonic disc and rapid growth of somites. ❑ This causes conversion of flat pear-shaped germ disc into a cylindrical embryo. ❑The head and tail ends of the disc remain relatively close together.The increased length of the disc causes it to bulge upward into the amniotic cavity. ❑With the formation of the head and tail folds, parts of the yolk sac become enclosed within the embryo. ❑ In this way, a tube lined by endoderm is formed in the embryo. This is the primitive gut, from which most of the gastrointestinal tract is derived. ❑ At first, the gut is in wide communication with the yolk sac. The part of the gut cranial to this communication is called the foregut; the part caudal to the communication is called the hindgut; while the intervening part is called the midgut . ❑The communication with the yolk sac becomes progressively narrower. As a result of these changes, the yolk sac becomes small and inconspicuous, and is now termed the definitive yolk sac (also called the umbilical vesicle). ❑The narrow channel connecting it to the gut is called the vitellointestinal duct (also called vitelline duct; yolk stalk or omphalomesenteric duct). This duct becomes elongated and eventually disappears. ❑With the formation of the cavity, the embryo (along with the amniotic cavity and yolk sac) remains attached to the trophoblast only by extraembryonic mesoderm into which the coelom does not exist. This extraembryonic mesoderm forms the connecting stalk. -
The Science of Amnioexcite™ Three Layer Placental Membrane Allograft
The Science of AmnioExcite™ Three Layer Placental Membrane Allograft REV. 10-2020 The Science of AmnioExcite™ Placental Membrane Allograft AmnioExcite™ is a full-thickness decellularized placental membrane. AmnioExcite™ is a lyophilized, full-thickness placental membrane allograft decellularized with LifeNet Health’s proprietary Matracell® process and patent pending technology and intended for homologous use as a barrier membrane.(1) Inclusion of the intact amniotic and chorionic membranes, as well as the trophoblast layer, makes it thicker than most available amniotic-only or amniotic-chorionic allografts, and provides a robust protective covering while also delivering superior handling. AmnioExcite™ retains the placental membrane’s naturally occurring growth factors, cytokines, protease inhibitors, and extracellular matrix components, such as proteoglycans, collagen and fibronectin(2) In vitro studies have shown that these endogenous factors are capable of inducing cellular proliferation and migration, mitigating inflammation, and inhibiting protein degradation(3-5) STRUCTURE OF THE THREE LAYER PLACENTAL MEMBRANE AMNIOTIC MEMBRANE CHORIONIC MEMBRANE TROPHOBLAST LAYER The placental membrane is comprised of the amnion and chorion (6). The amnion, also called amniotic membrane (AM) has five layers, including the epithelium, basement membrane, compact layer, fibroblast layer, and the spongy layer(6), which provide important extracellular membrane components, as well as a wide variety of growth factors, cytokines, and other proteins.(7) While these characteristics are important, the AM by itself lacks substantial structure for providing a protective covering and contains only a small portion of the biological factors found in the full-thickness placental membrane. AM-only grafts can also be difficult to apply and may migrate away from the intended site of application.(8) The chorion is comprised of four layers, including the cellular layer, reticular layer, the pseudobasement membrane and the trophoblast layer (TL) (6). -
The Law of Placenta
The Law of Placenta Mathilde Cohent ABSTRACT: Of the forms of reproductive labor in which legal scholars have been interested, placenta, the organ developed during pregnancy, has been overlooked. As placenta becomes an object of value for a growing number of individuals, researchers, clinicians, biobanks, and biotech companies, among others, its cultural meaning is changing. At the same time, these various constituencies may be at odds. Some postpartum parents and their families want to repossess their placenta for personal use, while third parties use placentas for a variety of research, medical, and commercial purposes. This Article contributes to the scholarship on reproductive justice and agency by asking who should have access to placentas and under what conditions. The Article emphasizes the insufficient protection the law affords pregnant people wishing to decide what happens to their placenta. Generally considered clinical waste under federal and state law, placental tissue is sometimes made inaccessible to its producers on the ground that it is infectious at the same time as it is made available to third parties on the ground that placenta is discarded and de-identified tissue. Less privileged people who lack the ability to shop for obstetric and other pregnancy-related services that allow them to keep their placentas are at a disadvantage in this chain of supply and demand. While calling for further research on the modus operandi of placenta markets and how pregnant people think about them, this Article concludes that lawmakers should take steps to protect decision-making autonomy over placental labor and offers a range of proposals to operationalize this idea.