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Egyptian doctors have discovered a rare condition known as "fetus in fetus" in a one-and-a-half-year-old girl, after gastrointestinal bleeding led to the detection of an unusual mass inside her stomach. It was found that the mass contained a malformed embryonic development, which is among the rare congenital conditions that develop when a twin is trapped inside the body of its sibling during the stages of fetal development. This condition usually appears within the first year of life. The mass was successfully surgically removed, and the child's condition stabilized after the operation. This case is considered extremely rare, with an estimated occurrence of just one case per 500,000 live births.
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