Medical Science







The Lamin Family of Proteins

Laminopathies are genetic disorders caused by mutations in the lamin family of nuclear proteins, lamin A/C. The LMNA gene encodes several lamin proteins, which are classified as type V intermediate filaments and make up the nuclear membrane. The various disorders…
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The Effects of Sex Polysomies on Anatomy

The most common polysomy involving the sex chromosomes is a disorder known as Klinefelter’s syndrome. Klinefelter’s results from the non-disjunction of one or more X chromomosomes during meiosis leading to an abnormal karyotype (chromosome number or structure). The majority of non-disjunction events…
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