A case of prolidase deficiency in a male patient.
Courtney N HallerJaya K George-AbrahamRosemary G PetersonLucia Z DiazPublished in: Pediatric dermatology (2021)
Prolidase deficiency is an extremely rare, autosomal recessive disorder resulting in defective collagen formation. We report a case of prolidase deficiency in a male child, highlighting the dermatologic features. Early diagnosis is important as these patients encounter significant multisystem comorbidities requiring multispecialty care.