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Isolated Protein C Deficiency in a Newborn
Clinical Laboratory
|May 5, 2023
Summary
Early diagnosis of congenital protein C deficiency is crucial for infants with purpura fulminans. Testing protein C levels in newborns and parents can improve outcomes for this rare thrombophilia.
Area of Science:
- Hematology
- Genetics
- Pediatrics
Background:
- Congenital protein C deficiency is a rare hereditary thrombophilia.
- Neonatal purpura fulminans represents the most severe manifestation of this deficiency.
- Early diagnosis is critical for improving patient prognosis.
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