Chromosomal Abnormalities

Chromosomal abnormalities are genetic changes that occur when an individual has the incorrect number or structure of chromosomes. These changes can manifest as physical anomalies and developmental disabilities, as well as an increased risk of certain diseases. Symptoms of chromosomal abnormalities vary depending on the type and severity of the abnormality, but can include short stature, intellectual disability, and infertility. Diagnosis is usually performed through a variety of tests such as karyotyping and chromosomal microarray. Although there is no cure for chromosomal abnormalities, they can be managed through supportive care, physical therapy, and education. Chromosomal abnormalities are a major cause of miscarriage and can lead to serious health problems, making it important to understand their cause and effects.

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Related Articles

7 article(s) found

Molecular Cytogenetic Investigations in a Novel Chromosomal Abnormality of t(10;15)(q22;q22) in a Pediatric Precursor-B-Acute Lymphoblastic Leukemia Patient

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Acquired Abnormalities of Plasma Von Willebrand Factor Related Parameters and ADAMTS13 Autoantibodies in Aggressive Haematological Malignancies.

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The Chromosomal and Functional Clustering of Markedly Divergent Human-Mouse Orthologs Run Parallel to their Compositional Features

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Annual Incidence Rate of Visual Field Abnormalities Determined by Frequency Doubling Technology Perimetry

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Morphological and Functional Abnormalities of the Thyroid Gland among End Stage Kidney Disease Patients

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Thyroid Function Abnormalities in Patients with Chronic Kidney Disease

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Cervico-Vaginal Smear Abnormalities in a Patient with Pemphigus Vulgaris

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