Works matching Trisomy 18 syndrome

Results: 571

Population-Based Analysis of Secular Trends in Age at Death in Trisomy 18 Syndrome in Japan from 1975 to 2016.

Published in:

Neonatology (16617800), 2021, v. 118, n. 1, p. 47, doi. 10.1159/000512922

By:

Suto, Maiko;
Isayama, Tetsuya;
Morisaki, Naho

Publication type:

Article

Anesthesia for children with complete trisomy 18 (Edwards syndrome): A cohort review of 84 anesthesia encounters in nine patients.

Published in:

Pediatric Anesthesia, 2021, v. 31, n. 4, p. 419, doi. 10.1111/pan.14131

By:

Birmingham, Erin E.;
Stucke, Astrid G.;
Diaz, Christina D.;
Veyckemans, Francis

Publication type:

Article

Reply to the Letter to the Editor "Underestimation of Trisomy 18 and 13 Syndromes in Vital Statistics from Inadequate Death Certificates".

Published in:

Neonatology (16617800), 2022, v. 119, n. 1, p. 135, doi. 10.1159/000520243

By:

Suto, Maiko;
Isayama, Tetsuya;
Takehara, Kenji;
Morisaki, Naho

Publication type:

Article

VACTERL Association with Meningomyelocele Combined with Trisomy 18 Syndrome.

Published in:

Neonatal Medicine, 2014, v. 21, n. 1, p. 74, doi. 10.5385/nm.2014.21.1.74

By:

Yu Kyong Kim;
Ji Hoon Lee;
Ga Won Jeon;
Jong Beom Sin

Publication type:

Article

Underestimation of Trisomy 18 and 13 Syndromes in Vital Statistics from Inadequate Death Certificates.

Published in:

2022

By:

Takashima, Kohei;
Hitosugi, Masahito

Publication type:

Letter

VACTERL associated with a rare limb anomaly combined with edward (trisomy 18) syndrome.

Published in:

Journal of Indian Association of Pediatric Surgeons, 2021, v. 26, n. 3, p. 206, doi. 10.4103/jiaps.JIAPS_237_20

By:

Hasan, Zaheer;
Thakur, Vinit;
Chaubey, Digamber;
Rahul, Sandip;
Kumar, Sujit

Publication type:

Article

Sequential integrated antenatal screening for Down’s syndrome, trisomy 18 and trisomy 13.

Published in:

Journal of Medical Screening, 2016, v. 23, n. 3, p. 116, doi. 10.1177/0969141315608895

By:

Bestwick, Jonathan P.;
Wald, Nicholas J.

Publication type:

Article

Antenatal screening for Down’s syndrome, trisomy 18, and trisomy 13: Reporting a single screening result for all three.

Published in:

Journal of Medical Screening, 2015, v. 22, n. 2, p. 100, doi. 10.1177/0969141315575545

By:

Bestwick, Jonathan P;
Wald, Nicholas J

Publication type:

Article

Letální syndromy v pediatrii – tři příběhy trizomie 18.

Published in:

Pediatrie pro Praxi, 2023, v. 24, n. 2, p. 111, doi. 10.36290/ped.2023.033

By:

Ducháčová, Michaela;
Pavlíček, Jan;
Pavlíčková, Eva;
Nowaková, Markéta;
Trávníček, Bořek;
Kuzníková, Iva;
Broďáková, Tereza

Publication type:

Article

Aberrant “Barbed-Wire” Nuclear Projections of Neutrophils in Trisomy 18 (Edwards Syndrome).

Published in:

2015

By:

Kahwash, Basil M.;
Nowacki, Nicholas B.;
Kahwash, Samir B.

Publication type:

Case Study

Aberrant “Barbed-Wire” Nuclear Projections of Neutrophils in Trisomy 18 (Edwards Syndrome).

Published in:

Case Reports in Hematology, 2015, p. 1, doi. 10.1155/2015/163857

By:

Kahwash, Basil M.;
Nowacki, Nicholas B.;
Kahwash, Samir B.

Publication type:

Article

Two-Dimensional Differential Gel Electrophoresis to Identify Protein Biomarkers in Amniotic Fluid of Edwards Syndrome (Trisomy 18) Pregnancies.

Published in:

PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0145908

By:

Hsu, Te-Yao;
Lin, Hao;
Hung, Hsuan-Ning;
Yang, Kuender D.;
Ou, Chia-Yu;
Tsai, Ching-Chang;
Cheng, Hsin-Hsin;
Chung, Su-Hai;
Cheng, Bi-Hua;
Wong, Yi-Hsun;
Chou, An Kuo;
Hsiao, Chang-Chun

Publication type:

Article

Antenatal detection of Edwards (Trisomy 18) and Patau (Trisomy 13) syndrome: England and Wales 2005-2012.

Published in:

Journal of Medical Screening, 2014, v. 21, n. 3, p. 113, doi. 10.1177/0969141314543128

By:

Springett, Anna L;
Morris, Joan K

Publication type:

Article

Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome.

Published in:

Hormone Research in Paediatrics, 2017, v. 87, n. 2, p. 130, doi. 10.1159/000448172

By:

MacMahon, Jayne M.;
O'Sullivan, Maureen J.;
McDermott, Michael;
Quinn, Feargal;
Morris, Thomas;
Green, andrew J.;
Betts, David R.;
O'Connell, Susan M.

Publication type:

Article

Single-cell chromatin accessibility landscape of human umbilical cord blood in trisomy 18 syndrome.

Published in:

Human Genomics, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s40246-021-00338-z

By:

Qiu, Xiaofen;
Yu, Haiyan;
Wu, Hongwei;
Hu, Zhiyang;
Zhou, Jun;
Lin, Hua;
Xue, Wen;
Cai, Wanxia;
Chen, Jiejing;
Yan, Qiang;
Dai, Weier;
Yang, Ming;
Tang, Donge;
Dai, Yong

Publication type:

Article

Trizomi 18 Sendromu: Olgu Sunumu.

Published in:

2012

By:

Karaman, Ali;
Kahveci, Hasan;
Laloğlu, Fuat

Publication type:

Case Study

Survival of children with trisomy 18 associated with the presence of congenital heart disease and intervention in the Republic of Korea.

Published in:

BMC Pediatrics, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12887-023-04056-4

By:

Song, In Gyu;
Shin, Seung Han;
Cho, Yoon-Min;
Lim, Youna

Publication type:

Article

Patau and Edwards Syndromes in a University Hospital: beyond palliative care.

Published in:

Revista Paulista de Pediatria, 2024, v. 42, p. 1, doi. 10.1590/1984-0462/2024/42/2023053

By:

Marçola, Ligia;
Zoboli, Ivete;
Verardo Polastrini, Rita Tiziana;
de Macedo Barbosa, Silvia Maria;
Cícero Falcão, Mário;
de Vicenzi Gaiolla, Paula

Publication type:

Article

Non‐surgical intervention for open myelomeningocele in an infant with trisomy 18.

Published in:

Pediatrics International, 2020, v. 62, n. 4, p. 496, doi. 10.1111/ped.14094

By:

Shitara, Yoshihiko;
Oida, Noriyasu;
Kondo, Utako;
Kushima, Reiko;
Omori, Isaku

Publication type:

Article

CONDUCTA MÉDICA FRENTE AL DIAGNÓSTICO PRENATAL DE TRISOMÍA 18: ¿SE APROXIMA UN CAMBIO DE PARADIGMA?

Published in:

Persona y Bioética, 2022, v. 26, n. 2, p. 1, doi. 10.5294/PEBI.2022.26.2.6

By:

Grimaux, Guadalupe;
Páez, Gustavo

Publication type:

Article

Future Perspectives in Oxidative Stress in Trisomy 13 and 18 Evaluation.

Published in:

Journal of Clinical Medicine, 2022, v. 11, n. 7, p. 1787, doi. 10.3390/jcm11071787

By:

Buczyńska, Angelika;
Sidorkiewicz, Iwona;
Hameed, Ahsan;
Krętowski, Adam Jacek;
Zbucka-Krętowska, Monika

Publication type:

Article

Palijativno kardiokirurško liječenje u djeteta s Edwardsovim sindromom.

Published in:

Lijecnicki Vjesnik, 2022, v. 144, p. 36, doi. 10.26800/LV-144-supl6-PS09

By:

Gržan, Dina;
Kulaš, Marjan;
Jukić, Lea;
Frković, Sanda Huljev

Publication type:

Article

First-trimester screening for trisomies 18 and 13, triploidy and Turner syndrome by detailed early anomaly scan.

Published in:

2016

By:

Wagner, P.;
Sonek, J.;
Hoopmann, M.;
Abele, H.;
Kagan, K. O.

Publication type:

journal article

Facial markers in second- and third-trimester fetuses with trisomy 18 or 13, triploidy or Turner syndrome.

Published in:

Ultrasound in Obstetrics & Gynecology, 2015, v. 46, n. 1, p. 60, doi. 10.1002/uog.14655

By:

Kagan, K. O.;
Sonek, J.;
Berg, X.;
Berg, C.;
Mallmann, M.;
Abele, H.;
Hoopmann, M.;
Geipel, A.

Publication type:

Article

Tricuspid regurgitation in screening for trisomies 21, 18 and 13 and Turner syndrome at 11+0 to 13+6 weeks of gestation.

Published in:

2009

By:

Kagan KO;
Valencia C;
Livanos P;
Wright D;
Nicolaides KH;
Kagan, K O;
Valencia, C;
Livanos, P;
Wright, D;
Nicolaides, K H

Publication type:

journal article

Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA.

Published in:

Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45438-1

By:

Rohrlach, Adam Benjamin;
Rivollat, Maïté;
de-Miguel-Ibáñez, Patxuka;
Moilanen, Ulla;
Liira, Anne-Mari;
Teixeira, João C.;
Roca-Rada, Xavier;
Armendáriz-Martija, Javier;
Boyadzhiev, Kamen;
Boyadzhiev, Yavor;
Llamas, Bastien;
Tiliakou, Anthi;
Mötsch, Angela;
Tuke, Jonathan;
Prevedorou, Eleni-Anna;
Polychronakou-Sgouritsa, Naya;
Buikstra, Jane;
Onkamo, Päivi;
Stockhammer, Philipp W.;
Heyne, Henrike O.

Publication type:

Article

Trisomy 18 syndrome with congenital fibrotic change in the liver.

Published in:

Pediatrics International, 2006, v. 48, n. 6, p. 646, doi. 10.1111/j.1442-200X.2006.02286.x

By:

Maruyama, Kenichi;
Koizumi, Takenobu;
Hirato, Junko

Publication type:

Article

Estimates for the sensitivity and false-positive rates for second trimester serum screening for Down syndrome and trisomy 18 with adjustment for cross-identification and double-positive results.

Published in:

Prenatal Diagnosis, 2001, v. 21, n. 1, p. 46, doi. 10.1002/1097-0223(200101)21:1<46::AID-PD984>3.0.CO;2-C

By:

Benn, Peter A.;
Ying, Jun;
Beazoglou, Tryfon;
Egan, James F. X.

Publication type:

Article

Second-trimester maternal serum inhibin A levels in fetal trisomy 18 and Turner syndrome with and without hydrops.

Published in:

Prenatal Diagnosis, 1998, v. 18, n. 10, p. 1061, doi. 10.1002/(SICI)1097-0223(199810)18:10<1061::AID-PD404>3.0.CO;2-M

By:

Lambert-Messerlian, G. M.;
Saller, D. N.;
Tumber, M. B.;
French, C. A.;
Peterson, C. J.;
Canick, J. A.

Publication type:

Article

HEAT-STABLE AND IMMUNOREACTIVE PLACENTAL ALKALINE PHOSPHATASE IN MATERNAL SERUM FROM DOWN'S SYNDROME AND TRISOMY 18 PREGNANCIES.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 11, p. 1051, doi. 10.1002/(SICI)1097-0223(199611)16:11<1051::AID-PD988>3.0.CO;2-T

By:

AITKEN, DAVID A.;
SYVERTSEN, BENTE S.;
CROSSLEY, JENNIFER A.;
BERRY, ESTHER;
CONNOR, J. MICHAEL

Publication type:

Article

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.

Published in:

Neuropathology, 2014, v. 34, n. 3, p. 219, doi. 10.1111/neup.12081

By:

Miyata, Hajime;
Miyata, Mio;
Ohama, Eisaku

Publication type:

Article

Follow up and evaluation of the Victorian first-trimester combined screening programme for Down syndrome and trisomy 18.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2007, v. 114, n. 7, p. 812, doi. 10.1111/j.1471-0528.2007.01349.x

By:

Jaques, A. M.;
Halliday, J. L.;
Francis, I.;
Bonacquisto, L.;
Forbes, R.;
Cronin, A.;
Sheffield, L. J.

Publication type:

Article

Significant improvement in survival outcomes of trisomy 18 with neonatal intensive care compared to non-intensive care: a single-center study.

Published in:

PeerJ, 2023, p. 1, doi. 10.7717/peerj.16537

By:

Shigeki Koshida;
Kentaro Takahashi

Publication type:

Article

Antenatal reflex DNA screening for trisomy 18 and trisomy 13 in addition to Down’s syndrome.

Published in:

Journal of Medical Screening, 2016, v. 23, n. 4, p. 171, doi. 10.1177/0969141315617982

By:

Bestwick, Jonathan P.;
Wald, Nicholas J.

Publication type:

Article

Evaluation of the intraoperative risk factors for esophageal anastomotic complications after primary repair of esophageal atresia with tracheoesophageal fistula.

Published in:

2016

By:

Okata, Yuichi;
Maeda, Kosaku;
Bitoh, Yuko;
Mishima, Yasuhiko;
Tamaki, Akihiko;
Morita, Keiichi;
Endo, Kosuke;
Hisamatsu, Chieko;
Fukuzawa, Hiroaki;
Yokoi, Akiko

Publication type:

journal article

Trysomy 18: an update on prenatal diagnosis and management. A case report.

Published in:

2017

By:

Dragan, I.;
Herghelegiu, C.;
Vladareanu, S.;
Moldoveanu, A.;
Oprescu, D.

Publication type:

Case Study

Evaluation of immunological abnormalities in patients with rare syndromes.

Published in:

Central European Journal of Immunology, 2022, v. 47, n. 4, p. 299, doi. 10.5114/ceji.2022.124080

By:

GUL, YAHYA;
KAPAKLI, HASAN;
AYTEKIN, SELMA EROL;
GUNER, ŞUKRU NAIL;
KELES, SEVGI;
GÜL ZAMANI, AYŞE;
YILDIRIM, MAHMUT SELMAN;
REISLI, ÏSMAIL

Publication type:

Article

Targeted fetal cell‐free DNA screening for aneuploidies in 4,594 pregnancies: Single center study.

Published in:

Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.678

By:

Koc, Altug;
Ozer Kaya, Ozge;
Ozyilmaz, Berk;
Kutbay, Yasar B.;
Kirbiyik, Ozgur;
Ozdemir, Taha R.;
Erdogan, Kadri M.;
Saka Guvenc, Merve;
Oztekin, Deniz C.;
Ozeren, Mehmet;
Pala, Halil G.;
Ekin, Atalay;
Gezer, Cenk;
Sahingoz Yildirim, Alkim G.;
Konuralp Atakul, Bahar;
Kurtulmus, Secil;
Turhan, Ugur;
Taner, Cuneyt E.

Publication type:

Article

P25.14: The utility of ultrasound examination in the prenatal diagnosis of a fetus with omfalocele, severe intrauterine growth restriction and mosaic trisomy 18 syndrome: case report.

Published in:

Ultrasound in Obstetrics & Gynecology, 2012, v. 40, p. 267, doi. 10.1002/uog.12107

By:

Oncescu, A.;
Albu, D.;
Albu, C.;
Enache, A.;
Enache, T.

Publication type:

Article

Ductus venosus Doppler in screening for trisomies 21, 18 and 13 and Turner syndrome at 11-13 weeks of gestation.

Published in:

Ultrasound in Obstetrics & Gynecology, 2009, v. 33, n. 5, p. 512, doi. 10.1002/uog.6330

By:

Maiz, N.;
Valencia, C.;
Kagan, K. O.;
Wright, D.;
Nicolaides, K. H.

Publication type:

Article

Microphthalmia in a Case of Edward Syndrome.

Published in:

Seminars in Ophthalmology, 2014, v. 29, n. 2, p. 114, doi. 10.3109/08820538.2013.874486

By:

Erginturk Acar, D.;
Acar, U.;
Ozdemir, O.;
Ozen, Z. T.;
Cakar, E. S.

Publication type:

Article

Trisomy 17 in a bonobo (Pan paniscus) and deletion of 3q in a lowland gorilla (Gorilla gorilla gorilla): comparison with human trisomy 18 and human deletion 4q syndrome.

Published in:

Cytogenetics & Cell Genetics, 2001, v. 95, n. 3/4, p. 228, doi. 10.1159/000059350

By:

Lear, T. L.;
Houck, M. L.;
Zhang, Y. W.;
Debnar, L. A.;
Sutherland-Smith, M. R.;
Young, L.;
Jones, K. L.;
Benirschke, K.

Publication type:

Article

Cardiac Surgical Repair Should Be Offered to Infants with Trisomy 18, Interrupted Aortic Arch and Ventricular Septal Defect.

Published in:

Journal of Law, Medicine & Ethics, 2016, v. 44, n. 2, p. 283, doi. 10.1177/1073110516654121

By:

Kavarana, Minoo N.

Publication type:

Article

Micrognathia as a Diagnosis Marker for the Prenatal Identification of Edwards Syndrome.

Published in:

Biomedicines, 2025, v. 13, n. 3, p. 573, doi. 10.3390/biomedicines13030573

By:

Albu, Cristina-Crenguţa;
Brăila, Anca Daniela;
Poalelungi, Cristian-Viorel;
Bohîltea, Laurenţiu-Camil;
Bănățeanu, Andreea-Mariana;
Damian, Constantin Marian;
Dîră, Laurențiu Mihai;
Bogdan-Andreescu, Claudia Florina

Publication type:

Article

Everyone has a story to tell: The experiences of grandparents with a grandchild diagnosed with a genetic life-limiting condition.

Published in:

International Journal of Birth & Parent Education, 2015, v. 2, n. 3, p. 16

By:

Brown, Erica

Publication type:

Article

Maternal Serum Screening for Down's Syndrome, Open Neural Tube Defects and Trisomy 18.

Published in:

Clinical Chemistry & Laboratory Medicine, 2001, v. 39, n. 6, p. 487

By:

Akbas, S. Halide;
Özben, Tomris;
Alper, Özgül;
Ugur, Aysegül;
Yücel, Gültekin;
Lüleci, Güven

Publication type:

Article

Detection of an Underlying 22q11.2 Duplication in a Female Neonate With Trisomy 18.

Published in:

Laboratory Medicine, 2017, v. 48, n. 4, p. 372, doi. 10.1093/labmed/lmx039

By:

Turbiville, Donald E.;
Hai Wu;
Jianli Dong

Publication type:

Article

Correlation of first-trimester thymus size with chromosomal anomalies.

Published in:

Journal of Perinatal Medicine, 2021, v. 49, n. 5, p. 604, doi. 10.1515/jpm-2020-0599

By:

Kleemann, Sarah;
Koch, Raphael;
Schmitz, Ralf;
Köster, Helen A.;
Braun, Janina;
Steinhard, Johannes;
Oelmeier, Kathrin;
Klockenbusch, Walter;
Möllers, Mareike

Publication type:

Article

Clinical Image: A Case of Edwards' Syndrome.

Published in:

Journal of Neonatology, 2023, v. 37, n. 3, p. 282, doi. 10.1177/09732179221143197

By:

Muppa, Vikas;
Kar, Shrutiprajna;
Sahoo, Tanushree;
Sahoo, Sanjukta

Publication type:

Article

Failure to diagnose Trisomy 18 (Edwards' syndrome) from antenatal scan.

Published in:: Clinical Risk, 2011, v. 17, n. 5, p. 199, doi. 10.1258/cr.2010.010036
Publication type:: Article