Abstract
D-penicillamine (D-PA) was first recognized as a potential benefit for neonatal hyperbilirubinemia (NHBI) caused by hemolytic diseases of the newborn infant or immaturity of UDP-glucuronyltransferase enzyme. During a long-term follow up study there was a remarkedly low incidence of retrolental fibroplasia (RLF) in the infants treated with D-PA in their neonatal period.
Highlights
D-PENICILLAMINE (D-PA) was first isolated as an amine from the degradation products of penicillin by Abraham, et al in 1942 [1]
During a long-term follow up study there was a remarkedly low incidence of retrolental fibroplasia (RLF) in the infants treated with D-PA in their neonatal period
All infants < 1500 g birthweight were treated with D-PA to prevent retinopathy of prematurity (ROP)
Summary
D-PENICILLAMINE (D-PA) was first isolated as an amine from the degradation products of penicillin by Abraham, et al in 1942 [1]. During a long-term follow up study there was a remarkedly low incidence of retrolental fibroplasia (RLF) in the infants treated with D-PA in their neonatal period.
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