SCHINZEL-GIEDION SYNDROME - RARE DESEASES

Schinzel-Giedion Syndrome



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Schinzel-Giedion syndrome is a rare congenital disease that causes the onset of skeletal malformations, changes in the face, obstruction of the urinary tract and severe developmental delays in the baby. Generally, Schinzel-Giedion Syndrome is not hereditary and, therefore, may occur in families with no history of the disease