Publications by authors named "Emmanouil M Karavitakis"

Article Synopsis
  • Recent research links mutations in the PLS3 gene to severe primary osteoporosis, chiefly in males due to its location on the X chromosome.
  • An 8-year-old boy exhibited severe osteoporosis symptoms, akin to osteogenesis imperfecta, prompting genetic testing, which ruled out other common mutations.
  • The identification of a new frameshift deletion in the PLS3 gene confirmed his diagnosis, emphasizing the need for PLS3 screening in patients with frequent fractures for accurate genetic counseling.
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Desmoplastic small round cell tumor (DSRCT) is a rare neoplasm with aggressive behavior. Usually it presents as a peritoneal mass, although other cases in various locations have been described. Since less than 10 cases of primary DSRCT in the pleura have been described, it is of interest to report a pediatric case arising from the pleura.

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