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A case of prolidase deficiency in a male patient.

Courtney N HallerJaya K George-AbrahamRosemary G PetersonLucia Z Diaz
Published 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.
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