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Klinefelter's Syndrome
A genetic condition affecting males, characterized by the presence of an extra X chromosome, which can lead to physical abnormalities and fertility issues.
Fragile X Syndrome
A genetic disorder characterized by intellectual disability, behavioral challenges, and distinctive physical features, caused by a mutation in the FMR1 gene.
Tay-Sachs Disease
A genetic disorder characterized by the destruction of nerve cells in the brain and spinal cord, leading to severe neurological impairment.
Sickle-Cell Anemia
A genetic blood disorder characterized by the production of abnormal, sickle-shaped red blood cells, causing various health complications.