Do specific ultrasonography features identified at the time of early pregnancy loss predict fetal chromosomal abnormality? – A systematic review and meta-analysis [PDF]
Genes and Diseases, 2019 To investigate the association of specific ultrasonography features identified during the diagnosis of early pregnancy loss (EPL) and abnormal karyotype. This was a systematic review and meta-analysis conducted in accordance with PRISMA criteria.
J. Huang +5 more
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Chromosomal abnormality variation detected by G‐banding is associated with prognosis of diffuse large B‐cell lymphoma treated by R‐CHOP‐based therapy [PDF]
Cancer Medicine, 2018 Diffuse large B‐cell lymphoma (DLBCL), which is the most prevalent disease subtype of non‐Hodgkin lymphoma, is highly heterogeneous in terms of cytogenetic and molecular features.
Yoshimi Mizuno +18 more
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Chromosomal Abnormality in Men with Impaired Spermatogenesis [PDF]
International Journal of Fertility and Sterility, 2014 Background: Chromosomal abnormalities and Y chromosome microdeletions are regarded as two most frequent genetic causes associated with failure of spermatogenesis in the Caucasian population.
Dana Mierla +2 more
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Down-Turner Syndrome: A Case with Double Monoclonal Chromosomal Abnormality [PDF]
Case Reports in Pediatrics, 2016 Introduction. The coexistence of Down and Turner syndromes due to double chromosome aneuploidy is very rare; it is even more rare to find the presence of a double monoclonal chromosomal abnormality. Objective. To report a unique case of double monoclonal
Gioconda Manassero-Morales +2 more
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Genetic counseling for a prenatal diagnosis of structural chromosomal abnormality with high-resolution analysis using a single nucleotide polymorphism microarray [PDF]
Clinics and Practice, 2016 A 41-year old pregnant woman underwent amniocentesis to conduct a conventional karyotyping analysis; the analysis reported an abnormal karyotype: 46,XY,add(9)(p24). Chromosomal microarray analysis (CMA) is utilized in prenatal diagnoses.
Akiko Takashima +2 more
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A Rare Chromosomal Abnormality in Chronic Lymphocytic Leukemia: t(13;13) [PDF]
Turkish Journal of Hematology, 2020 Akbar Safaei +2 more
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The assessment of holoprosencephaly cases in the last 10 years [PDF]
Ķazaķstannyṇ Klinikalyķ Medicinasy, 2021 Holoprosencephaly is a disorder of cleavage failure or incomplete differentiation of the forebrain structures. Chromosomal anomalies and environmental teratogenic factors play a role in its development. We reported 22 cases of holoprosencephaly diagnosed
Hulusi Goktug Gurer +2 more
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Advances in Biomedical and Health Sciences, 2022 Background: Male infertility is a global health issue that is poorly described in United Arab Emirates. Methods: In this 10-year retrospective cross-sectional study, we retrieved data of 312 male patients attending Dubai Fertility Center in United Arab ...
Ferdos Ebrahim, Ihsan Ali Mahasneh
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Proportion and Pattern of Chromosomal Abnormalities in Primary Amenorrhea in Kerala- A Retrospective Study [PDF]
Journal of Clinical and Diagnostic Research, 2022 Introduction: Primary amenorrhoea may be due to chromosomal abnormalities and identification of these abnormalities is important for counselling and management of these individuals.
Uma Thankam +6 more
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Journal of Human Reproductive Sciences, 2021 Background: Primary infertility is a common occurrence which affects approximately 15% of couples who desire to begin their family. Chromosomal abnormalities are well-established causes of pregnancy loss but may also have a role in explaining the cause ...
Paresh Singhal +5 more
doaj +1 more source