Works about TRISOMY 13 syndrome

Results: 118

Effectiveness of Fetal Medicine Foundation's Non-Biochemical Risk Calculation Algorithm in Detection of Common Trisomies Screening at 11–13 weeks of Gestation: 12 Years' Experience in Northern Thailand.

Published in:

International Journal of Women's Health, 2025, v. 17, p. 1693, doi. 10.2147/IJWH.S526271

By:

Kunanukulwatana, Chayanid;
Tongprasert, Fuanglada;
Luewan, Suchaya;
Tongsong, Theera

Publication type:

Article

Application of non-invasive prenatal testing for fetal chromosomal disorders in low-risk pregnancies: a follow-up study in central China.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1574775

By:

Huang, Qiuxiang;
Xu, Qiao;
Chen, Meihuan;
Fan, Wenli;
Huang, Hailong

Publication type:

Article

Morbidity and mortality following noncardiac surgical procedures among children with autosomal trisomy.

Published in:

Pediatric Anesthesia, 2022, v. 32, n. 5, p. 631, doi. 10.1111/pan.14415

By:

Matthews, Leslie J.;
Mpody, Christian;
Nafiu, Olubukola O.;
Tobias, Joseph D.

Publication type:

Article

Hallazgos clínicos inusuales en un paciente con síndrome de Patau.

Published in:

Revista Mexicana de Pediatria, 2024, v. 91, n. 5, p. 181, doi. 10.35366/120168

By:

Hugo Guapi-Nauñay, Victor;
Alejandro Mejía-Jiménez, Jonathan;
David Porras-Borja, Fabián

Publication type:

Article

Identification of Fetuses at Increased Risk of Trisomies in the First Trimester Using Axial Planes.

Published in:

Fetal Diagnosis & Therapy, 2024, v. 51, n. 1, p. 1, doi. 10.1159/000533879

By:

Montaguti, Elisa;
Diglio, Josefina;
Petrachi, Benedetta;
Arosio, Viola;
Fiorentini, Marta;
Cavalera, Marta;
Pellegrino, Anita;
Amodeo, Silvia;
Lenzi, Jacopo;
Pilu, Gianluigi

Publication type:

Article

Systematic Review of Accuracy Differences in NIPT Methods for Common Aneuploidy Screening.

Published in:

Journal of Clinical Medicine, 2025, v. 14, n. 8, p. 2813, doi. 10.3390/jcm14082813

By:

Marton, Tamas;
Erdélyi, Zsófia R.;
Takai, Minori;
Mészáros, Balázs;
Supák, Dorina;
Ács, Nándor;
Kukor, Zoltán;
Herold, Zoltan;
Hargitai, Beata;
Valent, Sándor

Publication type:

Article

Prenatal Diagnosis of Cleft Lip and Palate: A Retrospective Study.

Published in:

Journal of Clinical Medicine, 2024, v. 13, n. 16, p. 4804, doi. 10.3390/jcm13164804

By:

Brăila, Anca Daniela;
Damian, Constantin Marian;
Albu, Cristina-Crenguţa;
Botoacă, Oana;
Dȋră, Laurențiu Mihai;
Albu, Ştefan-Dimitrie;
Brăila, Matei Georgian;
Bănățeanu, Andreea-Mariana;
Poalelungi, Cristian-Viorel;
Bogdan-Andreescu, Claudia Florina

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

Cochlear Implantation in a Child with Patau Syndrome.

Published in:

Journal of International Advanced Otology, 2022, v. 18, n. 6, p. 541, doi. 10.5152/iao.2022.20074

By:

Çolpan, Bahar;
Ulusoy, Bülent

Publication type:

Article

Abortion Rate Following Chorionic Villous Sampling and Amniocentesis in Twin Pregnancies.

Published in:

Journal of Family & Reproductive Health, 2024, v. 18, n. 4, p. 269

By:

Golshahi, Fatemeh;
Rahimi-Sharbaf, Fatemeh;
Shirazi, Mahbobeh;
Saeedi, Sara;
Nejad, Athar Abdolrazagh;
Garfami, Sahar;
Saedi, Nafise;
Golshahi, Jafar;
Amiriarya, Zeynab;
Tavakolikia, Narjes;
Sahebdel, Behrokh

Publication type:

Article

Genetically induced abnormal cranial development in human trisomy 18 with holoprosencephaly: comparisons with the normal tempo of osteogenic-neural development.

Published in:

Journal of Anatomy, 2015, v. 227, n. 1, p. 21, doi. 10.1111/joa.12326

By:

Reid, Shaina N.;
Ziermann, Janine M.;
Gondré‐Lewis, Marjorie C.

Publication type:

Article

Quantitative and qualitative Ductus Venosus blood flow evaluation in the screening for Trisomy 18 and 13 -- suitability study.

Published in:

Ginekologia Polska, 2020, v. 91, n. 3, p. 144, doi. 10.5603/GP.2020.0031

By:

Czuba, Bartosz;
Nycz-Reska, Malgorzata;
Cnota, Wojciech;
Jagielska, Agnieszka;
Wloch, Agata;
Borowski, Dariusz;
Wegrzyn, Piotr

Publication type:

Article

A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal Ultrasound.

Published in:

Biomedicines, 2023, v. 11, n. 6, p. 1756, doi. 10.3390/biomedicines11061756

By:

Tang, Jiajie;
Han, Jin;
Xue, Jiaxin;
Zhen, Li;
Yang, Xin;
Pan, Min;
Hu, Lianting;
Li, Ru;
Jiang, Yuxuan;
Zhang, Yongling;
Jing, Xiangyi;
Li, Fucheng;
Chen, Guilian;
Zhang, Kanghui;
Zhu, Fanfan;
Liao, Can;
Lu, Long

Publication type:

Article

Does a High-Risk (>1/50) Result for First-Trimester Combined Screening Always Entail Invasive Testing? Which Patients from This Group Might Benefit from cfDNA Testing?

Published in:

Biomedicines, 2022, v. 10, n. 10, p. N.PAG, doi. 10.3390/biomedicines10102579

By:

García-Jiménez, Rocío;
Valero, Irene;
Corrales-Gutiérrez, Isabel;
Granell, Reyes;
Borrero, Carlota;
Sainz-Bueno, José Antonio

Publication type:

Article

A Rare Case of Neonatal Complicated Appendicitis in a Child with Patau's Syndrome.

Published in:

2014

By:

Pastore, Valentina;
Bartoli, Fabio

Publication type:

Case Study

A rare case of trisomy 13 mosaicism with only findings on first-trimester ultra- sound single umbilical artery and increased nuchal translucency.

Published in:

Hippokratia, 2024, v. 28, n. 1, p. 38

By:

A., Gerede;
M., Zafrakas;
P., Papasozomenou;
S., Papanikolopoulou;
A., Athanasiadis

Publication type:

Article

A newborn with trisomy 13 who had tetralogy of Fallot and metopic synostosis: Case report.

Published in:

2013

By:

Karabel, M.;
Yolbaş, I.;
Kelekçi, S.;
Şen, V.;
Haspolat, Y. K.;
Timuroğlu, L.

Publication type:

Case Study

A patient with Trisomy 13 mosaicism: review and case report.

Published in:

2015

By:

Mustaki, U.;
Jackson, S.

Publication type:

Conference Paper/Materials

Infant with trisomy 13 who developed acute elevation of intraocular pressure and glaucoma.

Published in:

Congenital Anomalies, 2020, v. 60, n. 5, p. 151, doi. 10.1111/cga.12367

By:

Yaginuma, Mizuki;
Sato, Takeshi;
Yuki, Kenya;
Hasegawa, Tomonobu

Publication type:

Article

Obstetric practice patterns in pregnancies complicated by fetal trisomy 13 or 18.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2018, v. 31, n. 18, p. 2441, doi. 10.1080/14767058.2017.1344638

By:

Dotters-Katz, Sarah K.;
Smid, Marcela C.;
Mcelwain, Cora;
Schulkin, Jay;
Kuller, Jeffrey A.

Publication type:

Article

Trisomy 13 and the risk of gestational hypertensive disorders: a population-based study.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2018, v. 31, n. 15, p. 1951, doi. 10.1080/14767058.2017.1332037

By:

Dotters-Katz, Sarah K.;
Humphrey, Whitney M.;
Senz, Kayli L.;
Lee, Vanessa R.;
Shaffer, Brian L.;
Kuller, Jeffrey A.;
Caughey, Aaron B.

Publication type:

Article

First trimester contingent screening for trisomies 21,18,13: is this model cost efficient and feasible in public health system?

Published in:

2017

By:

Colosi, Enrico;
D'Ambrosio, Valentina;
Periti, Enrico

Publication type:

journal article

Trisomy 13 with prenatally diagnosed congenital cystic adenomatoid malformation and hernia of the umbilical cord: A case report.

Published in:

2017

By:

Nakamura, Kohei;
Aoki, Showa;
Ishihara, Tomoko;
Nakayama, Kentaro;
Kanasaki, Haruhiko;
Kyo, Satoru

Publication type:

journal article

Patau syndrome.

Published in:

Paediatria Croatica, 2016, v. 60, n. 1, p. 27, doi. 10.13112/PC.2016.5

By:

Čulić, Vida;
Polić, Branka;
Mišković, Silvana;
Ivulić, Slavica Dragišić;
Zitko, Vanda;
Sipalo, Tatijana;
Pavelić, Jasminka

Publication type:

Article

Outcome after Prenatal Diagnosis of Trisomy 13, 18, and 21 in Fetuses with Congenital Heart Disease.

Published in:

Life (2075-1729), 2022, v. 12, n. 8, p. 1223, doi. 10.3390/life12081223

By:

Springer, Stephanie;
Karner, Eva;
Worda, Christof;
Grabner, Maria Magdalena;
Seidl-Mlczoch, Elisabeth;
Laccone, Franco;
Neesen, Jürgen;
Scharrer, Anke;
Ulm, Barbara

Publication type:

Article

Early assessment of clinical complexity and home care in patients affected by trisomy 13 and 18.

Published in:

European Journal of Pediatrics, 2025, v. 184, n. 3, p. 1, doi. 10.1007/s00431-025-06020-z

By:

Zanin, Anna;
Patti, Matteo;
Rosato, Isabella;
Divisic, Antuan;
Rusalen, Francesca;
Maghini, Irene;
Agosto, Caterina;
Benini, Franca

Publication type:

Article

Isolated trisomy 13 in refractory anemia with excess blasts: report of two cases and a brief literature review of this possible association.

Published in:

2016

By:

Mu, Qitian;
Chen, Ying;
Zhu, Huiling;
Zhang, Yi;
Wu, Ningning;
Lou, Yanru;
Shi, Songqiu;
Wu, Ying;
Shi, Cong;
Ouyang, Guifang

Publication type:

Case Study

Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin.

Published in:

Genes, 2022, v. 13, n. 11, p. 2027, doi. 10.3390/genes13112027

By:

Kleinfinger, Pascale;
Luscan, Armelle;
Descourvieres, Léa;
Buzas, Daniela;
Boughalem, Aicha;
Serero, Stéphane;
Valduga, Mylène;
Trost, Detlef;
Costa, Jean-Marc;
Vivanti, Alexandre J.;
Lohmann, Laurence

Publication type:

Article

Constitutional Mosaic Trisomy 13 in Two Germ Cell Layers is Different from Patau Syndrome? A Case Report.

Published in:

2016

By:

KUNWAR, FULESH;
PANDYA, VIDHI;
BAKSHI, SONAL R.

Publication type:

Case Study

THE MOST COMMON HUMAN AUTOSOMAL TRISOMIES.

Published in:

Studia Universitatis Babeş-Bolyai, Biologia, 2014, v. 59, n. 2, p. 123

By:

SZÉKELY, GYÖNGYI

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

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

Gene expression profiling and qRT-PCR expression of RRP1B, PCNT, KIF21A and ADRB2 in leucocytes of Down's syndrome subjects.

Published in:

Journal of Genetics, 2014, v. 93, p. 18, doi. 10.1007/s12041-012-0132-z

By:

SALEMI, MICHELE;
BARONE, CONCETTA;
ROMANO, CORRADO;
ZOLEZZI, FRANCESCA;
ROMANO, CARMELO;
SCAVUZZO, CATALDO;
SALLUZZO, ROBERTO;
SCILLATO, FRANCESCO;
SIGNORELLI, MARIA;
KAPETIS, DIMOS;
SALLUZZO, MARIA;
BOSCO, PAOLO

Publication type:

Article

Trisomies Reorganize Human 3D Genome.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 22, p. 16044, doi. 10.3390/ijms242216044

By:

Zhegalova, Irina V.;
Vasiluev, Petr A.;
Flyamer, Ilya M.;
Shtompel, Anastasia S.;
Glazyrina, Eugene;
Shilova, Nadezda;
Minzhenkova, Marina;
Markova, Zhanna;
Petrova, Natalia V.;
Dashinimaev, Erdem B.;
Razin, Sergey V.;
Ulianov, Sergey V.

Publication type:

Article

Role of Overexpressed Transcription Factor FOXO1 in Fatal Cardiovascular Septal Defects in Patau Syndrome: Molecular and Therapeutic Strategies.

Published in:

International Journal of Molecular Sciences, 2018, v. 19, n. 11, p. 3547, doi. 10.3390/ijms19113547

By:

Abuzenadah, Adel;
Alsaedi, Saad;
Karim, Sajjad;
Al-Qahtani, Mohammed

Publication type:

Article

Cross-sectional study of epidemiology of congenital anomaly of the hand in a tertiary care centre in India over 1 year.

Published in:

Indian Journal of Plastic Surgery, 2016, v. 49, n. 3, p. 424, doi. 10.4103/0970-0358.197231

By:

Mody, Nikunj B.;
Srinivasan, Shankar;
Thatte, Mukund

Publication type:

Article

Impact of abortion bans on pregnancies with severe life-limiting foetal anomalies in the United States: a cost-effectiveness analysis.

Published in:

European Journal of Contraception & Reproductive Health Care, 2025, v. 30, n. 3, p. 155, doi. 10.1080/13625187.2025.2469850

By:

Monroe, David M.;
Arora, Megha;
Bullard, Kimberley A.;
Caughey, Aaron B.

Publication type:

Article

Cell-Free DNA Analysis in Maternal Blood: Differences in Estimates between Laboratories with Different Methodologies Using a Propensity Score Approach.

Published in:

2019

By:

Bevilacqua, Elisa;
Jani, Jacques C.;
Letourneau, Alexandra;
Duiella, Silvia F.;
Kleinfinger, Pascale;
Lohmann, Laurence;
Resta, Serena;
Cos Sanchez, Teresa;
Fils, Jean-François;
Mirra, Marilyn;
Benachi, Alexandra;
Costa, Jean-Marc;
Jani, Jacques C;
Duiella, Silvia F;
Cos Sanchez, Teresa

Publication type:

journal article

Chromosome Cluster Type Identification Using a Swin Transformer.

Published in:

Applied Sciences (2076-3417), 2023, v. 13, n. 14, p. 8007, doi. 10.3390/app13148007

By:

Joshi, Indu;
Mondal, Arnab Kumar;
Navab, Nassir

Publication type:

Article

Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2021.811414

By:

Jing, Xiaosha;
Liu, Hongqian;
Zhu, Qian;
Liu, Sha;
Liu, Jianlong;
Bai, Ting;
Deng, Cechuan;
Xia, Tianyu;
Liu, Yunyun;
Cheng, Jing;
Wei, Xiang;
Xing, Lingling;
Luo, Yuan;
Zhou, Quanfang;
Chen, Lin;
Li, Lingping;
Wang, Jiamin

Publication type:

Article

Noninvasive Prenatal Screening Based on Second-Trimester Ultrasonographic Soft Markers in Low-Risk Pregnant Women.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.793894

By:

Liu, Yunyun;
Jing, Xiaosha;
Xing, Lingling;
Liu, Sha;
Liu, Jianlong;
Cheng, Jing;
Deng, Cechuan;
Bai, Ting;
Xia, Tianyu;
Wei, Xiang;
Luo, Yuan;
Zhou, Quanfang;
Zhu, Qian;
Liu, Hongqian

Publication type:

Article

HOW TO COMMUNICATE WITH A SPEECH IMPAIRED PERSON? A CASE STUDY OF A SUBJECT WITH MOSAIC PATAU SYNDROME.

Published in:

2014

By:

Rummo, Ingrid

Publication type:

Case Study

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

Holoprosencephaly in Patau Syndrome.

Published in:

Revista Paulista de Pediatria, 2023, v. 41, p. 1, doi. 10.1590/1984-0462/2023/41/2022027

By:

de Souza Schlosser, Amanda;
Coury Costa, Giovani José;
Salmazo da Silva, Henrique;
Menezes de Mello, Juan Luca;
de Oliveira Gomes, Lucy;
Oliveira Onoyama, Marina Michalski;
Coury Costa, Tatiana Martins

Publication type:

Article

Congenital diaphragmatic hernia and cleft lip and palate: looking for a common genetic etiology.

Published in:

Pediatric Surgery International, 2024, v. 40, n. 1, p. 1, doi. 10.1007/s00383-024-05843-5

By:

Nord, Petra;
Ebanks, Ashley H.;
Peterson, Petra;
Iwarsson, Erik;
Harting, Matthew T.;
Burgos, Carmen Mesas

Publication type:

Article

Accuracy of prenatal detection of facial clefts and relation between facial clefts, additional malformations and chromosomal abnormalities: a large referral-center cohort.

Published in:

Archives of Gynecology & Obstetrics, 2024, v. 309, n. 5, p. 1971, doi. 10.1007/s00404-023-07084-8

By:

Vibert, Florence;
Schmidt, Guel;
Löffler, Kerstin;
Gasiorek-Wiens, Adam;
Henrich, Wolfgang;
Verlohren, Stefan

Publication type:

Article

New osseous soft markers for trisomy 13, 18 and 21.

Published in:

2016

By:

Achter, Annika;
Hager, Thomas;
Fimmers, Rolf;
Gembruch, Ulrich;
Müller, Annette;
Müller, Annette M

Publication type:

journal article

ETHICS AND LEGAL ASPECT OF TERMINATION OF PREGNANCY WITH TRISOMY 13 (PATAU SYNDROME).

Published in:

Eduvest: Journal Of Universal Studies, 2023, v. 3, n. 3, p. 552, doi. 10.59188/eduvest.v3i3.769

By:

Ratna Dewi, Dian Andriani;
Darus, Febriansyah;
Avianggi, Hayra Diah;
Rusuldi, Gunawan;
Arifin Abidin, Sutan Finekri

Publication type:

Article

Graphical image of Trisomy Ultrascan related Total edge magic labelling.

Published in:

EAI Endorsed Transactions on Pervasive Health & Technology, 2024, v. 10, n. 1, p. 1, doi. 10.4108/eetpht.10.5311

By:

Pradeepa, A.;
Sundaram, O. V. Shanmuga;
Pushpalatha, N.

Publication type:

Article

Detection rates of a national fetal anomaly screening programme: A national cohort study.

Published in:

BJOG: An International Journal of Obstetrics & Gynaecology, 2023, v. 130, n. 1, p. 51, doi. 10.1111/1471-0528.17287

By:

Aldridge, Nicholas;
Pandya, Pranav;
Rankin, Judith;
Miller, Nicola;
Broughan, Jennifer;
Permalloo, Nadia;
McHugh, Annette;
Stevens, Sarah

Publication type:

Article