Parkinson's disease ranks among the top causes of global disability. Despite accessible treatments, their efficacy may diminish with time.
This study presents a unique case of Klinefelter syndrome, a chromosomal disorder characterized by a typical karyotype of 47, XXY, accompanied by a rare mosaic form of 47, XXY, and 48, XXXY, associated with various neurological manifestations.
In a startling revelation, researchers have reported the demise of a 72-year-old man in Amsterdam following an unprecedented 613-day encounter with COVID-19.
Aarskog syndrome also recognized as Aarskog-Scott Syndrome, Facio-digital-genital Syndrome, or Faciogenital Dysplasia, is a rare genetic disorder linked to the X chromosome, primarily affecting males.
Amy Rothfuss's 11-year-old son, referred to by his mother as Heratio (withheld his last name), suffers from fetal alcohol syndrome (FAS). This condition entails brain damage incurred during fetal development due to prenatal alcohol exposure.
Alkaptonuria is a rare genetic condition characterized by an overproduction of homogentisic acid, which accumulate pigment polymers throughout the body.
