Case report
Rare C1q deficiency presenting as pediatric SLE: A case study of two consanguineous siblings
Deficiencia rara de C1q que se presenta como LES pediátrico: estudio de caso de dos hermanos consanguíneos
Kerem Parlara, Berkay Aktaşa, Sena Ladin Sicakyüzb, Sezgin Şahinc, Özgür Kasapçopurc, Serdal Uğurlud,
Corresponding author
a Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey
b Acibadem University School of Medicine, Istanbul, Turkey
c Division of Pediatric Rheumatology, Department of Pediatrics, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey
d Division of Rheumatology, Department of Internal Medicine, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey
