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Osteogenesis imperfecta – The child with fragile bones
Osteogenesis imperfecta, also known as brittle bone disease, is a hereditary disorder characterized by the weakness and fragility of bones. The name refers to the nature of the disease, where the tissues of the bones are unable to regenerate properly, leading to frequent fractures. OI encompasses a complex group of disorders that include various types of hereditary defects and are associated with severe abnormalities in bone metabolism. The term “brittle bone” indicates the nature of the disease, as the bones of affected individuals are as fragile as glass. This condition is relatively rare, with estimates suggesting that only one in 30,000 newborns is affected, regardless of gender. The prevalence and…
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Twin in the Body? The Mystery of Teratoma
Tallós Rita’s case highlights the importance of gynecological screenings, as a routine examination revealed an unusual abnormality in the actress’s body. Based on the ultrasound conducted during the screening, her doctors reached a surprising conclusion: the hair of her deceased twin brother began to grow within the actress’s body. This finding is particularly striking, as there are several sets of twins in her family, and a cousin with similar symptoms had previously undergone surgery. The dark brown, solid mass of hair removed from the actress’s body was detected in time, so it did not cause any complaints and did not affect vital organs. Tallós Rita wants to emphasize that regular…
