Hereditary Heterozygous C2 Deficiency: Variable Clinical and Serological Manifestations Among Three Sisters.

doi:10.2174/1573397112666160808093031

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Article

Hereditary Heterozygous C2 Deficiency: Variable Clinical and Serological Manifestations Among Three Sisters.

Current rheumatology reviews - 1 Jan 2017

Yang Ji Wei, Rich Eric, Saint-Cyr Claire, Bourré-Tessier Josiane

Abstract excerpt

The causal link between inherited complement deficiencies and systemic lupus erythematosus (SLE) has been well established, although it remains a rare cause of the disease. We present the case of three biological sisters with hereditary heterozygous C2 deficiency, but who differ widely in their clinical and serological manifestations. Patient 1 is 25 years old and was diagnosed with SLE at the age of 12. Further...

Topics

Adult
Complement C2
Female
Humans
Lupus Erythematosus, Systemic
Phenotype
Siblings
Young Adult

Source

Open in PubMed

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PMID: 27502238
DOI: 10.2174/1573397112666160808093031

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

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