Works matching XYY syndrome

Results: 113

Autism spectrum disorders in XYY syndrome: two new cases and systematic review of the literature.

Published in:

European Journal of Pediatrics, 2014, v. 173, n. 3, p. 277, doi. 10.1007/s00431-014-2267-9

By:

Margari, Lucia;
Lamanna, Anna;
Craig, Francesco;
Simone, Marta;
Gentile, Mattia

Publication type:

Article

Diagnostic challenges of Marfan syndrome in an XYY young man.

Published in:

2012

By:

Lebreiro, Ana;
Martins, Elisabete;
Machado, José Carlos;
Abreu-Lima, Cassiano

Publication type:

Case Study

Sex chromosomes and the brain: a study of neuroanatomy in XYY syndrome.

Published in:

Developmental Medicine & Child Neurology, 2012, v. 54, n. 12, p. 1149, doi. 10.1111/j.1469-8749.2012.04418.x

By:

BRYANT, DANIEL M;
HOEFT, FUMIKO;
LAI, SONG;
LACKEY, JOHN;
ROELTGEN, DAVID;
ROSS, JUDITH;
REISS, ALLAN L

Publication type:

Article

Prader-Willi syndrome in a child with XYY.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 6, p. 412, doi. 10.1007/s100380050189

By:

Honma, A.;
Ishii, R.;
Ito, A.;
Kato, M.;
Saitoh, S.;
Hayasaka, K.

Publication type:

Article

XYY syndrome: a 13-year-old boy with tall stature.

Published in:

2015

By:

Won Ha Jo;
Mo Kyung Jung;
Ki Eun Kim;
Hyun Wook Chae;
Duk Hee Kim;
Ah Reum Kwon;
Ho-Seong Kim

Publication type:

Case Study

Possible contribution of XYY syndrome to neuroleptic malignant syndrome in a child receiving quetiapine.

Published in:

American Journal of Health-System Pharmacy, 2010, v. 67, n. 6, p. 459, doi. 10.2146/ajhp090091

By:

Randolph, Timothy C.

Publication type:

Article

Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome.

Published in:

Child: Care, Health & Development, 2024, v. 50, n. 5, p. 1, doi. 10.1111/cch.13324

By:

Zampini, Laura;
Zanchi, Paola;
Silibello, Gaia;
Mastromattei, Domenica;
Ajmone, Paola Francesca;
Dall'Ara, Francesca;
Monti, Federico;
Costantino, Maria Antonella;
Vizziello, Paola Giovanna

Publication type:

Article

Multifocal dysembryoplastic neuroepithelial tumour in a male with the XYY syndrome.

Published in:

Neuropathology & Applied Neurobiology, 2005, v. 31, n. 5, p. 556, doi. 10.1111/j.1365-2990.2005.00680.x

By:

Krossnes, B. K.;
Wester, K.;
Moen, G.;
Mørk, S. J.

Publication type:

Article

Myotonic dystrophy associated with 47 XYY syndrome.

Published in:

2000

By:

Asano, Atsutoshi;
Motomura, Naoyasu;
Yokota, Shingo;
Yoneda, Hiroshi;
Sakai, Toshiaki;
Tsutsumi, Shigetoshi

Publication type:

Case Study

Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report.

Published in:

2011

By:

Liao, Can;
Fu, Fang;
Zhang, Liang

Publication type:

journal article

Microspherophakia in a 47, XYY Syndrome Patient: A Case Report.

Published in:

Case Reports in Ophthalmology, 2020, v. 11, n. 1, p. 1, doi. 10.1159/000505058

By:

Rubalcava-Soberanis, Maria Lourdes;
Antonio-Aguirre, Bani;
Mendoza Velásquez, Cristina;
Perez-Ortiz, Andric Christopher;
Palacio-Pastrana, Claudia

Publication type:

Article

Severe regimen-related toxicity occurring in a patient with XYY syndrome receiving allogeneic peripheral blood stem cell transplantation.

Published in:

Annals of Hematology, 2002, v. 81, n. 7, p. 407, doi. 10.1007/s00277-002-0478-z

By:

Shibata, S.;
Kami, M.;
Kishi, Y.;
Hamaki, T.;
Ueyama, J.-i.;
Miyakoshi, S.;
Morinaga, S.-i.;
Hirabayashi, N.;
Kanda, Y.;
Mutou, Y.

Publication type:

Article

Oral, physical, and behavioral aspects of patient with chromosome 47, XYY syndrome.

Published in:

2015

By:

Scheidt, Lisa;
Sanabe, Mariane Emi;
Diniz, Michele Baffi

Publication type:

journal article

Contributions to auditory system conduction velocity: insights with multi-modal neuroimaging and machine learning in children with ASD and XYY syndrome.....

Published in:

Frontiers in Psychiatry, 2023, p. 1, doi. 10.3389/fpsyt.2023.105722

By:

Berman, Jerey I.;
Bloy, Luke;
Blaskey, Lisa;
Jackel, Carissa R.;
Miller, Judith S.;
Ross, Judith;
Edgar, J. Christopher;
Roberts, Timothy P. L.

Publication type:

Article

Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associations.

Published in:

2013

By:

Ulgiati, Fiorenza;
Nicita, Francesco;
Papetti, Laura;
Ursitti, Fabiana;
Di Maggio, Annalisa;
Tarani, Luigi;
Spalice, Alberto

Publication type:

journal article

Preferential Y-Y pairing and synapsis and abnormal meiotic recombination in a 47,XYY man with non obstructive azoospermia.

Published in:

Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-016-0218-z

By:

Caiyun Wu;
Liu Wang;
Furhan Iqbal;
Xiaohua Jiang;
Ihtisham Bukhari;
Tonghang Guo;
Gengxin Yin;
Cooke, Howard J.;
Zhenyi Cao;
Hong Jiang;
Qinghua Shi

Publication type:

Article

Deep phenotypic analysis of psychiatric features in genetically defined cohorts: application to XYY syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s11689-023-09476-y

By:

Raznahan, Armin;
Rau, Srishti;
Schaffer, Luke;
Liu, Siyuan;
Fish, Ari M.;
Mankiw, Catherine;
Xenophontos, Anastasia;
Clasen, Liv S.;
Joseph, Lisa;
Thurm, Audrey;
Blumenthal, Jonathan D.;
Bassett, Dani S.;
Torres, Erin N.

Publication type:

Article

Sensory Features as a Marker of Autism Spectrum Disorders.

Published in:

Journal of Autism & Developmental Disorders, 2020, v. 50, n. 6, p. 2240, doi. 10.1007/s10803-019-03948-8

By:

Bizzell, Ebonee;
Ross, Judith;
Rosenthal, Carly;
Dumont, Rachel;
Schaaf, Roseann

Publication type:

Article

Pneumoencephalographic and clinical findings of the XYY syndrome.

Published in:

Acta Psychiatrica Scandinavica, 1978, v. 58, n. 4, p. 360, doi. 10.1111/j.1600-0447.1978.tb00241.x

By:

Hakola, H. P. A.;
Iivanainen, M.

Publication type:

Article

Complete Testicular Feminization Syndrome with 47, XYY Karyotype: A Double Hit Phenomenon.

Published in:

Medical Principles & Practice, 1997, v. 6, n. 4, p. 216, doi. 10.1159/000157555

By:

Naguib, Kamal K.;
Al-Etreibi, Nabeel N.;
Al-Awadi, Sadika A.;
El-Harbi, Mohamed K.;
Kamal, Ahmed Saleh

Publication type:

Article

Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study.

Published in:

Journal of Intellectual Disability Research, 1998, v. 42, n. 1, p. 8, doi. 10.1046/j.1365-2788.1998.00091.x

By:

Weidmer-Mikhail;
Sheldon;
Ghaziuddin;
Mikhail, E. Weidmer

Publication type:

Article

Displasia ectodérmica hipohidrótica autosómica dominante. Reporte de un caso.

Published in:

2012

By:

Triviño F., Loreto;
Avaria E., Jaime;
Vargas F., María José;
Alarcón C., Rosario

Publication type:

Case Study

Reply to Herlihy and Halliday.

Published in:

2008

By:

Morris, Joan

Publication type:

Letter

Double Aneuploidy: A Case of Trisomy 21 with XYY.

Published in:

European Journal of General Medicine, 2011, v. 8, n. 4, p. 338, doi. 10.29333/ejgm/82767

By:

K”ken, Resit;
Bklmez, Aysegul;
Nadirgil K”ken, Glengl;
Eser, Betl;
Samlı, Hale;
Demir, Tevfik;
Solak, Mustafa

Publication type:

Article

Aneuploidy in Human Spermatozoa.

Published in:

Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 91, doi. 10.1159/000323795

By:

Templado, C.;
Vidal, F.;
Estop, A.

Publication type:

Article

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia.

Published in:

Developmental Medicine & Child Neurology, 2014, v. 56, n. 4, p. 346, doi. 10.1111/dmcn.12294

By:

Simpson, Nuala H;
Addis, Laura;
Brandler, William M;
Slonims, Vicky;
Clark, Ann;
Watson, Jocelynne;
Scerri, Thomas S;
Hennessy, Elizabeth R;
Bolton, Patrick F;
Conti‐Ramsden, Gina;
Fairfax, Benjamin P;
Knight, Julian C;
Stein, John;
Talcott, Joel B;
O'Hare, Anne;
Baird, Gillian;
Paracchini, Silvia;
Fisher, Simon E;
Newbury, Dianne F;
Consortium, SLI

Publication type:

Article

Asperger’s Disorder in an Adolescent With 47,XYY Chromosomal Syndrome.

Published in:

Clinical Pediatrics, 2011, v. 50, n. 6, p. 562, doi. 10.1177/0009922810380453

By:

Cashion, Larry;
Van Roden, Angela

Publication type:

Article

X- vs. Y-chromosome influences on human behavior: a deep phenotypic comparison of psychopathology in XXY and XYY syndromes.

Published in:

Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09574-5

By:

Schaffer, Lukas;
Rau, Srishti;
Larsen, Isabella G.;
Clasen, Liv;
Warling, Allysa;
Whitman, Ethan T.;
Nadig, Ajay;
McDermott, Cassidy;
Xenophontos, Anastasia;
Wilson, Kathleen;
Blumenthal, Jonathan;
Torres, Erin;
Raznahan, Armin

Publication type:

Article

Associated medical disorders and disabilities in children with autistic disorders.

Published in:

Autism: The International Journal of Research & Practice, 2004, v. 8, n. 1, p. 49, doi. 10.1177/1362361304040638

By:

Kielinen, Marko;
Rantala, Heikki;
Timonen, Eija;
Linna, Sirkka-Liisa;
Moilanen, Irma

Publication type:

Article

Modeling familial predictors of proband outcomes in neurogenetic disorders: initial application in XYY syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09360-7

By:

Wilson, Kathleen E.;
Fish, Ari M.;
Mankiw, Catherine;
Xenophontos, Anastasia;
Warling, Allysa;
Whitman, Ethan;
Clasen, Liv;
Torres, Erin;
Blumenthal, Jonathan;
Raznahan, Armin

Publication type:

Article

Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome.

Published in:

Journal of Neurodevelopmental Disorders, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s11689-018-9248-7

By:

Joseph, Lisa;
Farmer, Cristan;
Chlebowski, Colby;
Henry, Laura;
Fish, Ari;
Mankiw, Catherine;
Xenophontos, Anastasia;
Clasen, Liv;
Sauls, Bethany;
Seidlitz, Jakob;
Blumenthal, Jonathan;
Torres, Erin;
Thurm, Audrey;
Raznahan, Armin

Publication type:

Article

Primary male infertility in Kuwait: a cytogenetic and molecular study of 289 infertile Kuwaiti patients.

Published in:

Andrologia, 2007, v. 39, n. 3, p. 87, doi. 10.1111/j.1439-0272.2007.00769.x

By:

Mohammed, F.;
Al-Yatama, F.;
Al-Bader, M.;
Tayel, S. M.;
Gouda, S.;
Naguib, K. K.

Publication type:

Article

A patient with 46,XY/47,XYY karyotype and female phenotype: a case report.

Published in:

BMC Endocrine Disorders, 2020, v. 20, n. 1, p. 1, doi. 10.1186/s12902-020-0523-8

By:

Liu, Zhi-Hui;
Zhou, Shi-Chao;
Du, Jun-Wen;
Zhang, Kun;
Wu, Tao

Publication type:

Article

PHYSIQUE IN CHROMOSOMAL DISORDERS.

Published in:

Papers on Anthropology, 2006, v. 15, p. 28

By:

Buday, József

Publication type:

Article

Pregnancies with positive non-invasive prenatal testing result for sex chromosome abnormalities in a tertiary hospital in Hong Kong.

Published in:

Hong Kong Journal of Gynaecology, Obstetrics & Midwifery, 2022, v. 22, n. 2, p. 87, doi. 10.12809/hkjgom.22.2.07

By:

SO, P. L.;
Lai, S.;
WONG, P. P.;
SIONG, K. H.;
LEUNG, H. K.;
SIN, W. K.;
KAN, Anita S. Y.;
LUK, H. M.;
LO, Ivan F. M.;
YEUNG, K. C. A. U.;
WONG, S. F.

Publication type:

Article

Trisomy 9p syndrome and XYY syndrome in siblings.

Published in:

Clinical Genetics, 1977, v. 11, n. 1, p. 67, doi. 10.1111/j.1399-0004.1977.tb01280.x

By:

Gustavson, K.-H.;
Wahlström, J.

Publication type:

Article

Down's syndrome with additional XYY aneuploidy.

Published in:

Clinical Genetics, 1975, v. 8, n. 1, p. 55, doi. 10.1111/j.1399-0004.1975.tb01954.x

By:

Leary, P. M.;
Webb, P. M.;
Melzer, C. W.;
Close, H. G.

Publication type:

Article

Cytogenetics, hormones and behavior disability: comparison of XYY and XXY syndromes.

Published in:

Clinical Genetics, 1974, v. 6, n. 5, p. 370, doi. 10.1111/j.1399-0004.1974.tb02260.x

By:

Money, John;
Annecillo, Charles;
Orman, Barry Van;
Borgaonkar, Digamber S.

Publication type:

Article

An XYY baby with Prader syndrome.

Published in:

Clinical Genetics, 1974, v. 6, n. 4, p. 323, doi. 10.1111/j.1399-0004.1974.tb02093.x

By:

Iinuma, Kazuso;
Tanae, Ayako;
Tanaka, Goro

Publication type:

Article

The XYY Syndrome: Reality or Myth?

Published in:

Clinical Genetics, 1974, v. 5, n. 5, p. 387, doi. 10.1111/j.1399-0004.1974.tb01711.x

By:

Noël, B.;
Duport, J. P.;
Revil, D.;
Dussuyer, I.;
Quack, B.

Publication type:

Article

The XYY syndrome in an adolescent male exhibiting prominent behavioral problems.

Published in:

Clinical Genetics, 1972, v. 3, n. 3, p. 162, doi. 10.1111/j.1399-0004.1972.tb01454.x

By:

Alam, M. T.;
Deschamps, R.;
Gaba, E.;
Kasatiya, S. S.;
Grant, W. F.

Publication type:

Article

Prenatal Diagnosis of Sex Chromosome Abnormalities: The 8-Year Experience of a Single Medical Center.

Published in:

Fetal Diagnosis & Therapy, 2008, v. 23, n. 1, p. 76, doi. 10.1159/000109231

By:

Vaknin, Zvi;
Reish, Orit;
Ben-Ami, Ido;
Heyman, Eli;
Herman, Arie;
Maymon, Ron

Publication type:

Article

A unique association of Noonan syndrome and 47,XYY syndrome in a male presenting with failure to thrive.

Published in:

2017

By:

Bellfield, Edward J.;
Shad, Zohra

Publication type:

Case Study

THE XYY OFFENDER: A MODERN MYTH?

Published in:

Journal of Criminal Law, Criminology & Police Science, 1971, v. 62, n. 1, p. 59, doi. 10.2307/1142122

By:

Fox, Richard G.

Publication type:

Article

Acute promyelocytic leukaemia with a PML-RARA insertional translocation and a chromosome 21 abnormality in XYY syndrome: Case report.

Published in:

Journal of International Medical Research, 2014, v. 42, n. 6, p. 1363, doi. 10.1177/0300060514540630

By:

He, Yi;
Li, Xudong;
Wang, Dongning;
Zhang, Erhong;
Hu, Yuan;
Wang, Wenwen;
Huang, Renwei;
Xiao, Ruozhi

Publication type:

Article

Stimulant medication in 47,XYY syndrome: a report of two cases.

Published in:

2005

By:

Anne Ruud;
Peter Arnesen;
Liv Larsen Stray;
Stéphane Vildalen;
Per Vesterhus

Publication type:

Case Study

Brain morphology in children with 47, XYY syndrome: a voxel- and surface-based morphometric study.

Published in:

Genes, Brain & Behavior, 2014, v. 13, n. 2, p. 127, doi. 10.1111/gbb.12107

By:

Lepage, J.‐F.;
Hong, D. S.;
Raman, M.;
Marzelli, M.;
Roeltgen, D. P.;
Lai, S.;
Ross, J.;
Reiss, A. L.

Publication type:

Article

Biogenic Amines in 47, XYY Syndrome.

Published in:

Neuropsychobiology, 1978, v. 4, n. 6, p. 366, doi. 10.1159/000117653

By:

Bioulac, B.;
Benezech, M.;
Renaud, B.;
Roche, D.;
Noël, B.

Publication type:

Article

Rare Genomic Rearrangement in a Boy with Williams-Beuren Syndrome Associated to XYY Syndrome and Intriguing Behavior.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3197, doi. 10.1002/ajmg.a.37360

By:

Dutra, Roberta L.;
Piazzon, Flavia B.;
Zanardo, Évelin A.;
Costa, Thais Virginia Moura Machado;
Montenegro, Marília M.;
Novo‐Filho, Gil M.;
Dias, Alexandre T.;
Nascimento, Amom M.;
Kim, Chong Ae;
Kulikowski, Leslie D.

Publication type:

Article

Spontaneous resolution of cystic hygroma in 47,XYY fetus.

Published in:

2007

By:

Phupong, Vorapong;
Sittisomwong, Tul

Publication type:

journal article