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Chromosomal Abnormalities

 Chromosomal Abnormalities

Chromosome abnormalities refer to structural or numerical changes in chromosomes that can disrupt normal genetic function, leading to developmental disorders, congenital abnormalities, and various genetic diseases. These abnormalities may arise from errors in cell division, such as nondisjunction or chromosomal breakage, resulting in conditions like Down syndrome, Turner syndrome, Klinefelter syndrome, and various deletion or duplication syndromes. Understanding chromosome abnormalities is essential for genetic counseling, prenatal diagnosis, disease risk assessment, and research in cytogenetics and molecular genetics.

Chromosome abnormalities, chromosomal disorders, chromosomal mutations, aneuploidy, structural chromosome abnormalities, nondisjunction, deletion syndrome, duplication syndrome, translocation, inversion, cytogenetics, karyotyping, prenatal diagnosis, genetic testing, genomic instability, Down syndrome, Turner syndrome, Klinefelter syndrome, trisomy, monosomy

#ChromosomeAbnormalities, #ChromosomalDisorders, #ChromosomalMutations, #GeneticDisorders, #Aneuploidy, #Cytogenetics, #GeneticsResearch, #GenomicInstability, #GeneticTesting, #PrenatalDiagnosis, #Karyotyping, #DownSyndrome, #TurnerSyndrome, #KlinefelterSyndrome, #TrisomyConditions, #Monosomy, #StructuralAbnormalities, #GeneticHealth, #HumanGenetics, #MedicalGenetics

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