Woman with Turner syndrome and her child with acute leukemia (a case report)
Summary. Turner syndrome (TS) is a chromosomal condition that affects development in females. The case of TS in the mother whose child was diagnosed with acute leukemia at the age of 1.5 years is presented. FANCI gene in child was detected among 94 genes associated with hematologic malignancies. Ac...
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Дата: | 2023 |
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PH Akademperiodyka
2023
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oai:ojs2.ex.aqua-time.com.ua:article-1632023-10-11T16:43:48Z Woman with Turner syndrome and her child with acute leukemia (a case report) Woman with Turner syndrome and her child with acute leukemia (a case report) Kitsera, N. Dorosh, O. Makukh, H. acute leukemia., phenotype, reproductive history, Turner syndrome acute leukemia., phenotype, reproductive history, Turner syndrome Summary. Turner syndrome (TS) is a chromosomal condition that affects development in females. The case of TS in the mother whose child was diagnosed with acute leukemia at the age of 1.5 years is presented. FANCI gene in child was detected among 94 genes associated with hematologic malignancies. Acute lymphoblastic leukemia, common-B ІІ, L1, associated with t(12;21)(p13;q22), TEL/AML1 (ETV6/RUNX1) in a child was detected during a prophylactic examination. During the treatment of the baby, the mother had a second pregnancy, which ended in miscarriage at 8 weeks. Upon cytogenetic examination in the mother TS was revealed — mos45,Х[23]/46, ХХ[7], and the father’s karyotype was without abnormalities (46, ХУ). After chemotherapy, the child is in clinical-hematological remission. It could be suggested that chromosomal abnormalities in mother with TS may cause the chromosomal instability and hematological malignancy in offspring. Summary. Turner syndrome (TS) is a chromosomal condition that affects development in females. The case of TS in the mother whose child was diagnosed with acute leukemia at the age of 1.5 years is presented. FANCI gene in child was detected among 94 genes associated with hematologic malignancies. Acute lymphoblastic leukemia, common-B ІІ, L1, associated with t(12;21)(p13;q22), TEL/AML1 (ETV6/RUNX1) in a child was detected during a prophylactic examination. During the treatment of the baby, the mother had a second pregnancy, which ended in miscarriage at 8 weeks. Upon cytogenetic examination in the mother TS was revealed — mos45,Х[23]/46, ХХ[7], and the father’s karyotype was without abnormalities (46, ХУ). After chemotherapy, the child is in clinical-hematological remission. It could be suggested that chromosomal abnormalities in mother with TS may cause the chromosomal instability and hematological malignancy in offspring. PH Akademperiodyka 2023-05-30 Article Article application/pdf https://exp-oncology.com.ua/index.php/Exp/article/view/2020-4-18 10.32471/exp-oncology.2312-8852.vol-42-no-4.15275 Experimental Oncology; Vol. 42 No. 4 (2020): Experimental Oncology; 333-336 Експериментальна онкологія; Том 42 № 4 (2020): Експериментальна онкологія; 333-336 2312-8852 1812-9269 10.32471/exp-oncology.2312-8852.vol-42-no-4 en https://exp-oncology.com.ua/index.php/Exp/article/view/2020-4-18/2020-4-18 Copyright (c) 2023 Experimental Oncology https://creativecommons.org/licenses/by-nc/4.0/ |
institution |
Experimental Oncology |
baseUrl_str |
|
datestamp_date |
2023-10-11T16:43:48Z |
collection |
OJS |
language |
English |
topic |
acute leukemia. phenotype reproductive history Turner syndrome |
spellingShingle |
acute leukemia. phenotype reproductive history Turner syndrome Kitsera, N. Dorosh, O. Makukh, H. Woman with Turner syndrome and her child with acute leukemia (a case report) |
topic_facet |
acute leukemia. phenotype reproductive history Turner syndrome acute leukemia. phenotype reproductive history Turner syndrome |
format |
Article |
author |
Kitsera, N. Dorosh, O. Makukh, H. |
author_facet |
Kitsera, N. Dorosh, O. Makukh, H. |
author_sort |
Kitsera, N. |
title |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
title_short |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
title_full |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
title_fullStr |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
title_full_unstemmed |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
title_sort |
woman with turner syndrome and her child with acute leukemia (a case report) |
title_alt |
Woman with Turner syndrome and her child with acute leukemia (a case report) |
description |
Summary. Turner syndrome (TS) is a chromosomal condition that affects development in females. The case of TS in the mother whose child was diagnosed with acute leukemia at the age of 1.5 years is presented. FANCI gene in child was detected among 94 genes associated with hematologic malignancies. Acute lymphoblastic leukemia, common-B ІІ, L1, associated with t(12;21)(p13;q22), TEL/AML1 (ETV6/RUNX1) in a child was detected during a prophylactic examination. During the treatment of the baby, the mother had a second pregnancy, which ended in miscarriage at 8 weeks. Upon cytogenetic examination in the mother TS was revealed — mos45,Х[23]/46, ХХ[7], and the father’s karyotype was without abnormalities (46, ХУ). After chemotherapy, the child is in clinical-hematological remission. It could be suggested that chromosomal abnormalities in mother with TS may cause the chromosomal instability and hematological malignancy in offspring. |
publisher |
PH Akademperiodyka |
publishDate |
2023 |
url |
https://exp-oncology.com.ua/index.php/Exp/article/view/2020-4-18 |
work_keys_str_mv |
AT kitseran womanwithturnersyndromeandherchildwithacuteleukemiaacasereport AT dorosho womanwithturnersyndromeandherchildwithacuteleukemiaacasereport AT makukhh womanwithturnersyndromeandherchildwithacuteleukemiaacasereport |
first_indexed |
2025-07-17T12:16:00Z |
last_indexed |
2025-07-17T12:16:00Z |
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