A Child with Partial Trisomy 4 (q26 – qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death

التفاصيل البيبلوغرافية
العنوان: A Child with Partial Trisomy 4 (q26 – qterminal) Resulting from Paternally Inherited Translocation (4:18) Associated with Multiple Congenital Anomalies and Death
المؤلفون: Debarshi Roy, Shu Wen Koh, Swatishree Padhi, Manoor Prakash Hande, Birendranath Banerjee, Abhik Chakraborty, Santosh Panda, Nirmal Kumar Mohakud
المصدر: Genome Integrity
بيانات النشر: Wolters Kluwer - Medknow, 2019.
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Proband, congenital, hereditary, and neonatal diseases and abnormalities, Offspring, Aneuploidy, Chromosomal translocation, Case Report, Biology, 03 medical and health sciences, 0302 clinical medicine, Meiosis, Genetics, medicine, multicolor fluorescence in situ hybridization, Balanced translocation, Molecular Biology, 030219 obstetrics & reproductive medicine, omphalocele, medicine.diagnostic_test, Karyotype, karyotyping, medicine.disease, 030104 developmental biology, Chromosome 4, Fluorescence in situ hybridization
الوصف: Parental balanced reciprocal translocations can result in partial aneuploidy in the offspring due to unbalanced meiotic segregation during gametogenesis. Herein, we report the phenotypic and cytogenetic characterization in a 9-day-old male child with partial trisomy of chromosome 4. Karyotyping of the proband and parents was performed along with multicolor fluorescence in situ hybridization (mFISH) of paternal chromosomes. Conventional cytogenetic analysis by karyotyping showed 47,XY,der(18),t(4;18)(q26;q22),+4 in proband, and the paternal karyotype was found as 47,XY,der(18),t(4;18)(q26;q22). mFISH analysis on paternal chromosomal preparations confirmed both region and origin of the balanced translocation. In this study, karyotyping helped us to identify both numerical and structural anomalies in the proband, and mFISH helped us to confirm our cytogenetic findings. Therefore, cytogenetic screening of both partners is recommended before pregnancy to rule out or confirm the presence of any numerical or structural anomaly in one, both, or none of the partners.
اللغة: English
تدمد: 2041-9414
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6a5b46d183427a6115192e7b1b68e6dTest
http://europepmc.org/articles/PMC6540766Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....b6a5b46d183427a6115192e7b1b68e6d
قاعدة البيانات: OpenAIRE