Fetal Hydantoin Syndrome (FHS) is a condition that occurs in babies who have been exposed to the medication phenytoin (also known as Dilantin) during pregnancy. Phenytoin is commonly prescribed to treat epilepsy and certain other neurological disorders. Unfortunately, the use of this medication during pregnancy can have detrimental effects on the developing fetus, leading to the development of Fetal Hydantoin Syndrome.
The primary cause of Fetal Hydantoin Syndrome is the exposure of the developing fetus to phenytoin. When a pregnant woman takes phenytoin, the drug crosses the placenta and reaches the developing baby. The medication interferes with the normal growth and development of various organs and systems, resulting in a range of physical and cognitive abnormalities in the affected child.
There are several factors that contribute to the severity and likelihood of Fetal Hydantoin Syndrome:
The manifestations of Fetal Hydantoin Syndrome can vary widely from one affected individual to another. Common physical features include facial abnormalities (such as a broad nasal bridge, cleft lip or palate, and widely spaced eyes), growth deficiencies, and limb abnormalities. Additionally, individuals with FHS may experience developmental delays, intellectual disabilities, learning difficulties, and behavioral problems.
Early diagnosis and intervention are crucial for managing Fetal Hydantoin Syndrome. If a pregnant woman is taking phenytoin, it is essential for her to work closely with her healthcare provider to monitor the medication's dosage and potential risks to the developing baby. After birth, a thorough evaluation by a medical team can help identify and address any physical or developmental issues promptly.