Works matching Triple X syndrome

Results: 89

Triple X Syndrome Woman Presenting as Premature Ovarian Failure.

Published in:

International Journal of Infertility & Fetal Medicine, 2013, v. 4, n. 3, p. 96, doi. 10.5005/jp-journals-10016-1070

By:

Chandana, C.;
Venkatesh, Shreedhar

Publication type:

Article

The psychiatric phenotype in triple X syndrome: New hypotheses illustrated in two cases.

Published in:

Developmental Neurorehabilitation, 2012, v. 15, n. 3, p. 233, doi. 10.3109/17518423.2012.655799

By:

Otter, Maarten;
Schrander-Stumpel, Constance T. R. M.;
Didden, Robert;
Curfs, Leopold M. G.

Publication type:

Article

Cross-sectional study shows that impaired bone mineral status and metabolism are found in nonmosaic triple X syndrome.

Published in:

2017

By:

Stagi, Stefano;
Di Tommaso, Mariarosaria;
Scalini, Perla;
Sandini, Elena;
Masoni, Fabrizio;
Chiarelli, Francesco;
Verrotti, Alberto;
Giglio, Sabrina;
Romano, Silvia;
Martino, Maurizio

Publication type:

journal article

Jejunal atresia in an infant with triple-X syndrome.

Published in:

2004

By:

Trautner, M. C.;
Aladangady, N.;
Maalouf, E.;
Misra, D.

Publication type:

journal article

Schizencephaly in triple-X syndrome.

Published in:

Pediatrics International, 2001, v. 43, n. 3, p. 296, doi. 10.1046/j.1442-200X.2001.01382.x

By:

Ehara, Hiroaki;
Eda, Isematsu

Publication type:

Article

High Myopia Associated with Triple X Syndrome.

Published in:

2016

By:

Nishi, Tomo;
Ogata, Nahoko

Publication type:

Case Study

Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Published in:

2010

By:

Lalatta, Faustina;
Quagliarini, Donatella;
Folliero, Emanuela;
Cavallari, Ugo;
Gentilin, Barbara;
Castorina, Pierangela;
Forzano, Francesca;
Forzano, Serena;
Grosso, Enrico;
Viassolo, Valeria;
Naretto, Valeria;
Gattone, Stefania;
Ceriani, Florinda;
Faravelli, Francesca;
Gargantini, Luigi;
Naretto, Valeria Giorgia

Publication type:

journal article

Premature ovarian aging in primary infertility: Triple X syndrome.

Published in:

Journal of Human Reproductive Sciences, 2011, v. 4, n. 3, p. 153, doi. 10.4103/0974-1208.92292

By:

Kodandapani, Sreelakshmi;
Pai, Muralidhar V.;
Nambiar, Jayaraman;
Moka, Rajshekar

Publication type:

Article

A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome.

Published in:

Turkish Journal of Hematology, 2014, v. 31, n. 2, p. 184, doi. 10.4274/tjh.2013.0064

By:

Hanjun Kim;
Sang Sun Hwang;
Young Uh;
Juwon Kim;
Kap Jun Yoon;
Ji-yong Lee

Publication type:

Article

Triple X syndrome: a review of the literature.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 3, p. 265, doi. 10.1038/ejhg.2009.109

By:

Otter, Maarten;
Schrander-Stumpel, Constance T. R. M.;
Curfs, Leopold M. G.

Publication type:

Article

A Case of Triple X Syndrome Manifesting with the Syndrome of NonverbalLearning Disabilities.

Published in:

Child Neuropsychology, 1998, v. 4, n. 3, doi. 10.1076/chin.4.3.225.3179

By:

Ryan, Thomas V;
Crews Jr., David W;
Cowen, Lawrence;
Goering, Aeron M;
Barth, Jeffrey T

Publication type:

Article

A case of torsion of a mucinous cystadenoma in triple-X syndrome with pure gonadal dysgenesis.

Published in:

Archives of Gynecology & Obstetrics, 2006, v. 274, n. 3, p. 174, doi. 10.1007/s00404-005-0116-9

By:

Jeong-Heon Lee;
Kwan-Sik Kim;
Yong-Gon Cho

Publication type:

Article

PRADER-WILLI SYNDROME WITH ASSOCIATED TRIPLE-X MOSAICISM.

Published in:

Acta Endocrinologica (1841-0987), 2010, v. 6, n. 4, p. 521, doi. 10.4183/aeb.2010.521

By:

Pascanu, I.;
Ruff, R.;
Banescu, C.;
Skrypnyk, C.

Publication type:

Article

Autism in association with Triple X syndrome.

Published in:

2012

By:

Ali, Syed;
Byrne, Nollaig;
Mulligan, Aisling

Publication type:

Letter

Novel biallelic ATM mutations coexist with a mosaic form of triple X syndrome in an 11-year-old girl at remission after T cell acute leukemia.

Published in:

2018

By:

Sharapova, Svetlana O.;
Valochnik, Alena V.;
Guryanova, Irina E.;
Sakovich, Inga S.;
Aleinikova, Olga V.

Publication type:

Case Study

GENETIC SYNDROMES AS A CAUSE OF TREATMENT RESISTANCE IN SCHIZOPHRENIA: A CASE WITH TRIPLE X SYNDROME.

Published in:

Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2019, v. 82, n. 3, p. 162, doi. 10.26650/IUITFD.2019.0011

By:

TURAN, Bahadır;
AKINCI, Mehmet Akif;
ESİN, İbrahim Selçuk;
DURSUN, Onur Burak

Publication type:

Article

Aplastic Anemia in Triple X Syndrome.

Published in:

Children, 2023, v. 10, n. 1, p. 100, doi. 10.3390/children10010100

By:

Aldarwish, Mohammed;
Alaithan, Israa;
Alawami, Fatimah

Publication type:

Article

Craniofacial and dental manifestations of triple X syndrome associated with congenital hypothyroidism: a case report.

Published in:

Special Care in Dentistry, 2014, v. 34, n. 3, p. 156, doi. 10.1111/scd.12050

By:

Ferrazzo, Kívia Linhares;
Payeras, Marcia Rodrigues;
Ferrazzo, Vilmar Antonio;
Mezomo, Maurício Barbieri

Publication type:

Article

Mixed Hyperlipidemia Associated with Triple X Syndrome (A Case Report).

Published in:

Romanian Journal of Diabetes Nutrition & Metabolic Diseases, 2014, v. 21, n. 2, p. 103, doi. 10.2478/rjdnmd-2014-0015

By:

Anton-Pǎduraru, Dana-Teodora;
Oltean, Carmen;
Trandafir, Laura Mihaela;
Rusu, Cristina

Publication type:

Article

Evaluating the Scope of Language Impairments in a Patient with Triple X Syndrome: A Brief Report.

Published in:

Developmental Neurorehabilitation, 2020, v. 23, n. 6, p. 402, doi. 10.1080/17518423.2020.1764652

By:

van Elst, Puck Christine;
Otter, Maarten;
Wijnen, Frank;
Junge, Caroline

Publication type:

Article

Triple X syndrome: Psychiatric disorders and impaired social functioning as a risk factor.

Published in:

European Psychiatry, 2023, v. 66, n. 1, p. 1, doi. 10.1192/j.eurpsy.2022.2355

By:

Otter, Maarten;
Campforts, Bea C. M.;
Stumpel, Constance T. R. M.;
van Amelsvoort, Thérèse A. M. J.;
Drukker, Marjan

Publication type:

Article

Brain structure in triple X syndrome: regional gray matter volume and cortical thickness in adult women with 47,XXX karyotype.

Published in:

Journal of Neurodevelopmental Disorders, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s11689-025-09608-6

By:

Domes, Gregor;
Croyé, Marie-Anne;
Freilinger, Petra;
Bohlscheid, Andreas;
Willinek, Winfried A.;
Meyer, Jobst

Publication type:

Article

Тризомия Х - клинични случаи.

Published in:

Pediatria, 2024, v. 64, n. 1, p. 43

By:

Халваджиян, И.;
Младенов, В.;
Ковачева, К.;
Петрова, Ч.;
Йотова, В.

Publication type:

Article

Dysgerminoma of the ovary in a patient with triple-X syndrome.

Published in:

1995

By:

Kemp, B.;
Hauptmann, S.;
Schröder, W.;
Amo-Takyi, B.;
Leeners, B.;
Rath, W.;
Schröder, W

Publication type:

journal article

Intestinal Atresia, Encephalocele, and Cardiac Malformations in Infants with 47,XXX: Expansion of the Phenotypic Spectrum and a Review of the Literature.

Published in:

Fetal Diagnosis & Therapy, 2010, v. 27, n. 2, p. 113, doi. 10.1159/000284929

By:

Bağci, Soyhan;
Müller, Andreas;
Franz, Axel;
Heydweiller, Andreas;
Berg, Christoph;
Nöthen, Markus M.;
Bartmann, Peter;
Reutter, Heiko

Publication type:

Article

Anesthesia and Triple X Syndrome.

Published in:

2012

By:

Norton, Kim

Publication type:

Case Study

The Turner syndrome in patient with 45X/47XXX mosaic karyotype – case report.

Published in:

2015

By:

Maciejewska-Jeske, Marzena;
Czyzyk, Adam;
Meczekalski, Blazej

Publication type:

Case Study

Dysgerminoma of the ovary in a patient with triple-X syndrome (47, XXX) and Marfanoid habitus features.

Published in:

Ginekologia Polska, 2021, v. 92, n. 6, p. 466, doi. 10.5603/GP.2021.0106

By:

Moskwinska, Karolina;
Sniadecki, Marcin;
Wydra, Dariusz

Publication type:

Article

Rare case of massive congenital bilateral chylothorax in a hydropic fetus with true mosaicism 47, XXX/46, XX.

Published in:

Journal of Obstetrics & Gynaecology Research, 2014, v. 40, n. 1, p. 259, doi. 10.1111/jog.12131

By:

Cremonini, Giorgio;
Poggi, Alice;
Capucci, Roberta;
Vesce, Fortunato;
Patella, Alfredo;
Marci, Roberto

Publication type:

Article

Sella Turcica Shape in Fragile X Syndrome.

Published in:

In Vivo, 2021, v. 35, n. 6, p. 3581, doi. 10.21873/invivo.12662

By:

FRIEDRICH, REINHARD E.

Publication type:

Article

Triple X Syndrome with a Rare Finding: Cleft Palate.

Published in:

Journal of Pediatric Research, 2018, v. 5, n. 2, p. 100, doi. 10.4274/jpr.32154

By:

Gürkaş, Esra;
Genç, Hülya Maraş;
Kılıç, Esra

Publication type:

Article

Structural and numerical changes of chromosome X in patients with esophageal atresia.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 9, p. 1077, doi. 10.1038/ejhg.2013.295

By:

Brosens, Erwin;
de Jong, Elisabeth M;
Barakat, Tahsin Stefan;
Eussen, Bert H;
D'haene, Barbara;
De Baere, Elfride;
Verdin, Hannah;
Poddighe, Pino J;
Galjaard, Robert-Jan;
Gribnau, Joost;
Brooks, Alice S;
Tibboel, Dick;
de Klein, Annelies

Publication type:

Article

Goltz Syndrome Combined with Triple X Syndrome, a Case Report.

Published in:

Cleft Palate Craniofacial Journal, 2024, v. 61, n. 3, p. 534, doi. 10.1177/10556656221141236

By:

Sone, Itaru;
Honda, Takayuki;
Sakuraba, Minoru;
Satoh, Kazuro;
Kuwajima, Yukinori;
Baba, Shunsuke;
Wada, Yasunori

Publication type:

Article

Ollier's disease associated with ovarian juvenile granulosa cell tumor and triple X syndrome: A letter to the editor.

Published in:

Journal of Research in Medical Sciences, 2022, v. 27, n. 5, p. 41, doi. 10.4103/jrms.jrms_980_21

By:

Shafieyoon, Shamim;
Tahririan, Mohammad;
Hekmatnia, Ali;
Zarei, Andrew;
Hekmatnia, Farzaneh;
Soufi, Ghazaleh

Publication type:

Article

Chromosomal abnormalities predisposing to infertility, testing, and management: a narrative review.

Published in:

Bulletin of the National Research Centre, 2021, v. 45, n. 1, p. 1, doi. 10.1186/s42269-021-00523-z

By:

Yahaya, Tajudeen O.;
Oladele, Esther O.;
Anyebe, Daniel;
Obi, Chidiebere;
Bunza, M. D. A.;
Sulaiman, Ridwan;
Liman, Usman U.

Publication type:

Article

Genomic imbalances in pediatric patients with chronic kidney disease.

Published in:

Journal of Clinical Investigation, 2015, v. 125, n. 5, p. 2171, doi. 10.1172/JCI80877

By:

Verbitsky, Miguel;
Sanna-Cherchi, Simone;
Fasel, David A.;
Levy, Brynn;
Kiryluk, Krzysztof;
Wuttke, Matthias;
Abraham, Alison G.;
Kaskel, Frederick;
Köttgen, Anna;
Warady, Bradley A.;
Furth, Susan L.;
Wong, Craig S.;
Gharavi, Ali G.

Publication type:

Article

Cytogenetic evaluation of patients with clinical spectrum of Turner syndrome.

Published in:

Journal of Human Reproductive Sciences, 2013, v. 6, n. 2, p. 129, doi. 10.4103/0974-1208.117177

By:

Moka, Rajasekhar;
Sreelakshmi, Kodandapani;
Gopinath, Puthiya Mundyat;
Satyamoorthy, Kapettu

Publication type:

Article

Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.

Published in:

Cytogenetic & Genome Research, 2005, v. 111, n. 2, p. 179, doi. 10.1159/000086390

By:

Liehr, T.;
Mrasek, K.;
Starke, H.;
Claussen, U.;
Schreiber, G.

Publication type:

Article

EP04.12: Triple X syndrome associated with central nervous system anomalies and cardiac anomaly.

Published in:

Ultrasound in Obstetrics & Gynecology, 2015, v. 46, p. 197, doi. 10.1002/uog.15550

By:

Sahin Uysal, N.;
Gulumser, C.;
Yanik, F.F.

Publication type:

Article

Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome family.

Published in:

Human Genetics, 2011, v. 129, n. 5, p. 513, doi. 10.1007/s00439-010-0944-y

By:

Draaken, Markus;
Giesen, Carmen A.;
Kesselheim, Anne L.;
Jabs, Ronald;
Aretz, Stefan;
Kugaudo, Monika;
Chrzanowska, Krystyna H.;
Krajewska-Walasek, Malgorzata;
Ludwig, Michael

Publication type:

Article

Triple X superwomen: their post-compulsory education and employability.

Published in:

Journal of Education & Work, 2021, v. 34, n. 1, p. 81, doi. 10.1080/13639080.2021.1875126

By:

Attfield, Kate

Publication type:

Article

Tall Stature as Presenting Symptom in a Girl with Triple X Syndrome.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2003, v. 16, n. 2, p. 233, doi. 10.1515/jpem.2003.16.2.233

By:

Liebezeit, B. U.;
Rohrer, T. R.;
Singer, H.;
Doerr, H. G.

Publication type:

Article

Central Precocious Puberty in a Girl with Triple X Syndrome and Neonatal Diabetes Mellitus Associated with Paternal Isodisomy of Chromosome 6.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 7, p. 897, doi. 10.1515/jpem.2001.14.7.897

By:

Valerio, G.;
Franzese, A.;
Palmieri, A.;
Mackay, D. J. G.;
Gardner, R. J.;
Temple, I. K.

Publication type:

Article

Synergistic Effects of Extra X Chromosome on Development of Systemic Lupus Erythematosus and Sjögren Disease in Klinefelter and Triple X Syndrome: A Retrospective Cohort Study.

Published in:

ACR Open Rheumatology, 2025, v. 7, n. 1, p. 1, doi. 10.1002/acr2.11778

By:

Palmer, Anna‐Kay;
Tan, Irene J.

Publication type:

Article

The Triple X Chromosome Syndrome in Childhood: Recent Empirical Findings.

Published in:

Child Development, 1983, v. 54, n. 4, p. 831, doi. 10.2307/1129888

By:

Rovet, Joanne;
Netley, Charles

Publication type:

Article

Behavioral and psychological features in girls and women with triple‐X syndrome.

Published in:

American Journal of Medical Genetics. Part A, 2018, v. 176, n. 11, p. 2284, doi. 10.1002/ajmg.a.40477

By:

Freilinger, Petra;
Kliegel, David;
Hänig, Susann;
Oehl‐Jaschkowitz, Barbara;
Henn, Wolfram;
Meyer, Jobst

Publication type:

Article

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.

Published in:

American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2870, doi. 10.1002/ajmg.a.37688

By:

Wigby, Kristen;
D'Epagnier, Cheryl;
Howell, Susan;
Reicks, Amy;
Wilson, Rebecca;
Cordeiro, Lisa;
Tartaglia, Nicole

Publication type:

Article

A Case of Triple-X Syndrome with Situs Inversus Totalis.

Published in:

Turkiye Klinikleri Journal of Medical Sciences, 2013, v. 33, n. 2, p. 588, doi. 10.5336/medsci.2011-26702

By:

İKBAL, Mevlit;
EKER, Hatice KOÇAK;
TOS, Tülay;
ÇEBİ, Alper Han;
ALP, Muhammed Yunus

Publication type:

Article

Social functioning and emotion recognition in adults with triple X syndrome.

Published in:

BJPsych Open, 2021, v. 7, n. 2, p. 1, doi. 10.1192/bjo.2021.8

By:

Otter, Maarten;
Crins, Peter M. L.;
Campforts, Bea C. M.;
Stumpel, Constance T. R. M.;
van Amelsvoort, Thérèse A. M. J.;
Vingerhoets, Claudia

Publication type:

Article

Atypical Rett syndrome in a girl with mosaic triple X and MECP2 variant.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 3, p. 1, doi. 10.1002/mgg3.1122

By:

Takahashi, Satoru;
Takeguchi, Ryo;
Kuroda, Mami;
Tanaka, Ryosuke

Publication type:

Article