Chromosome Abnormalities

Chromosome abnormalities are changes in the structure or number of chromosomes. Chromosomes are packages of genetic material found in every cell of the human body and determine an individual's physical characteristics. Abnormalities can be caused by missing or extra parts, or abnormal rearrangements of genetic material. These abnormalities can result in a wide range of physical, mental, and medical conditions. They can be inherited from parents, but can also occur spontaneously. Chromosome abnormalities may cause infertility, learning disabilities, and birth defects, among other medical issues. Early diagnosis and treatment are important for optimizing development and minimizing health complications. With advances in genetic technology, researchers continue to gain a better understanding of the causes and potential treatments for chromosome abnormalities.

← Journal of Chromosomes

Related Articles

11 article(s) found

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

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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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Pericentric Inversion in Chromosome 10 in a Girl, Inherited from a Phenotypically Normal Mother: Case Report and Literature Review

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Humans Chromosome 1 Fractal Periods Signature is Highly Correlated with Intelligence and Brain Evolution

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Intriguing Humans and Primates chromosomes 4

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An Inherited Balanced Translocation Between Chromosomes 4 and 6 in Recurrent Pregnancy Loss: A Case Report

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Thyroid Function Abnormalities in Patients with Chronic Kidney Disease

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A Patient with Monoclonal Gammopathy of Undetermined Significance and Detected Philadelphia Chromosome

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Cervico-Vaginal Smear Abnormalities in a Patient with Pemphigus Vulgaris

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The Chromosomes of Dictyostelium Giganteum

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