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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,
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

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Rare C1q deficiency presenting as pediatric SLE: A case study of two consanguineous siblings

Kerem Parlar, Berkay Aktaş, Sena Ladin Sicakyüz, Sezgin Şahin, Özgür Kasapçopur, Serdal Uğurlu
10.1016/j.reumae.2025.501843
Reumatol Clin. 2025;21:
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Reumatología Clínica (English Edition)
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