𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Systemic lupus erythematosus with C1q deficiency

✍ Scribed by N.M. Stone; A. Williams; J.D. Wilkinson; G. Bird


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
255 KB
Volume
142
Category
Article
ISSN
0007-0963

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

We report a case of systemic lupus erythematosus associated with C1q deficiency. Our patient presented at the age of 6 years with cutaneous lupus. She later developed Raynaud’s phenomenon, non-scarring alopecia, oral ulceration and grand mal seizures due to cerebral vasculitis. Complement C3 and C4 levels were consistently normal during flares of her lupus and haemolytic activity of her complement was absent, suggesting a deficiency of an early component of the complement cascade. No C1q could be detected.


πŸ“œ SIMILAR VOLUMES


The C1q binding assay in systemic lupus
✍ Robert D. Inman; J. K. K. Fong; B. A. Pussell; P. J. Ryan; Graham R. V. Hughes πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 438 KB

## Abstract To investigate the relationship of C1q binding assay (C1qBA) to disease activity in systemic lupus erythematosus (SLE), a retrospective study was carried out on 232 C1qBA performed in 33 patients with SLE. When initial values only were assessed (33 tests in 33 patients), there was no re

Homozygous hereditary C1q deficiency and
✍ Jason H. Slingsby; Peter Norsworthy; Glen Pearce; Akshay K. Vaishnaw; Helen Issl πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 739 KB

Objective. To describe a new kindred with Clq deficiency and to identify the molecular lesions responsible for complete functional Clq deficiency in this and 2 other previously described kindreds. Methods. The A-, B-, and C-chain genes of Clq were amplified by polymerase chain reaction, cloned, and