Propylthiouracil embryofetopathy

Propylthiouracil embryofetopathy is a rare teratologic disease characterized by variable congenital anomalies resulting from maternal treatment and prenatal exposure to propylthiouracil. Anomalies frequently encountered include ear malformations (e.g. accessory auricle, preauricular sinus/fistula/cyst), urinary system malformations (e.g. isolated unilateral kidney, congenital hydronephrosis), gastrointestinal anomalies (e.g. congenital bands with intestinal malrotation) and cardiac defects (e.g. situs inversus dextrocardia, cardiac outflow tract defects).

Also known as: PTU embryofetopathy, PTU embryopathy, propylthiouracil embryopathy

0 clinical trials for this condition and its sub-types, 0 tagged with Propylthiouracil embryofetopathy itself.