نتایج جستجو برای: balanced chromosomal rearrangement

تعداد نتایج: 116705  

2015
Anne-Claude Tabet Alain Verloes Marion Pilorge Elsa Delaby Richard Delorme Gudrun Nygren Françoise Devillard Marion Gérard Sandrine Passemard Delphine Héron Jean-Pierre Siffroi Aurelia Jacquette Andrée Delahaye Laurence Perrin Céline Dupont Azzedine Aboura Pierre Bitoun Mary Coleman Marion Leboyer Christopher Gillberg Brigitte Benzacken Catalina Betancur

BACKGROUND Apparently balanced chromosomal rearrangements can be associated with an abnormal phenotype, including intellectual disability and autism spectrum disorder (ASD). Genome-wide microarrays reveal cryptic genomic imbalances, related or not to the breakpoints, in 25% to 50% of patients with an abnormal phenotype carrying a microscopically balanced chromosomal rearrangement. Here we perfo...

Journal: :journal of reproduction and infertility 0

uterine leiomyomas/fibroids are the most common pelvic tumors of the female genital tract. the initiators remaining unknown, estrogens and progesterone are considered as promoters of fibroid growth. fibroids are monoclonal tumors showing 40-50% karyo-typically detectable chromosomal abnormalities. cytogenetic aberrations involving chromosomes 6, 7, 12 and 14 constitute the major chromosome abno...

Journal: :American journal of medical genetics 1994
M McDonald S Maynard S Sheldon J Innis

This is the first reported case of an unbalanced chromosome rearrangement resulting in trisomy 5q35.5-->qter and monosomy 16p 13.3-->pter, in a boy with mental and growth retardation, minor anomalies, and a history of bilateral papillary thyroid carcinoma. This was the result of a familial balanced translocation. The clinical and cytogenetic manifestations of the case are presented and the poss...

2012
Ahmadreza Zarifian Zeinab Farhoodi Roya Amel Salmeh Mirzaee Mohammad Hassanzadeh-Nazarabadi

One of the major causes of spontaneous abortion before the fourth month of pregnancy is chromosomal abnormalities. We report an unusual case of a familial balanced chromosomal translocation in a consanguineous couple who experienced 4 spontaneous abortions. Chromosomal studies were performed on the basis of G-banding technique at high resolution and revealed 46, XX, t (16; 6) (p12; q26) and 46,...

Journal: :Genome research 2013
Caroline Robberecht Thierry Voet Masoud Zamani Esteki Beata A Nowakowska Joris R Vermeesch

Large-scale analysis of balanced chromosomal translocation breakpoints has shown nonhomologous end joining and microhomology-mediated repair to be the main drivers of interchromosomal structural aberrations. Breakpoint sequences of de novo unbalanced translocations have not yet been investigated systematically. We analyzed 12 de novo unbalanced translocations and mapped the breakpoints in nine....

2008
M. Hassanzadeh Nazarabadi R. Raoofian R. Abutorabi

The most significant complication of pregnancy is recurrent miscarriage. Numerous factors have been described as associations with recurrent wastage such as: uterine abnormalities, immunological factors, endocrinologic imbalance and chromosomal defects. Cytogenetic evaluation of couples with recurrent pregnancy losses is performed on the basis of G-banding technique only after other possible et...

Claudia Behrend, Javad Karimzad Hagh, Mir Davood Omrani, Mitra Ansari Dezfouli, Sadaf Omori Sarabi, Seyed Behrooz Mohseni, Seyed Khalil Rashidi,

Background: Mosaicism of a normal cell population and an unbalanced autosomal chromosome rearrangement is rarely seen. If the abnormal cell line contributes to a minor part of soma, the phenotype is expected to be normal. Case Report: We report a 29-year-old woman who had balance chromosomal translocation of 46,XX,t(5;21) with a 2-year-old affected girl, characterized by mental retardation, dys...

2015
Hannie Kartapradja Nanis Sacharina Marzuki Mark D. Pertile David Francis Lita Putri Suciati Helena Woro Anggaratri Debby Dwi Ambarwati Firman Prathama Idris Harry Lesmana Hidayat Trimarsanto Chrysantine Paramayuda Alida Roswita Harahap

We report an exceptional complex chromosomal rearrangement (CCR) found in three individuals in a family that involves 4 chromosomes with 5 breakpoints. The CCR was ascertained in a phenotypically abnormal newborn with additional chromosomal material on the short arm of chromosome 4. Maternal karyotyping indicated that the mother carried an apparently balanced CCR involving chromosomes 4, 6, 11,...

Journal: :Genetics and molecular research : GMR 2016
H G Zhang X Y Zhang H Y Zhang T Tian S B Xu R Z Liu

Balanced translocation is a common structural chromosomal rearrangement in humans. Carriers can be phenotypically normal but have an increased risk of pregnancy loss, fetal death, and the transmission of chromosomal abnormalities to their offspring. Existing prenatal screening technologies and diagnostic procedures fail to detect balanced translocation, so genetic counseling for carriers remain...

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