congenital erythropoietic porphyria n.
Enhanced porphyrin formation by erythroid cells in bone marrow, leading to severe porphyrinuria, often with hemolytic anemia and persistent cutaneous photosensitivity. Also called Günther’s disease.
- Congenital generalized fibromatosis
congenital generalized fibromatosis n. A rare disorder that is often fatal in the first week of life, although sometimes undergoing spontaneous remission, characterized by multiple subcutaneous and visceral fibrous tumors that are present at birth.
- Congenital glaucoma
congenital glaucoma n. See buphthalmia.
- Congenital hemolytic anemia
congenital hemolytic anemia n. See hereditary spherocytosis.
- Congenital hemolytic jaundice
congenital hemolytic jaundice n. See hereditary spherocytosis.