Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Cutaneous manifestations of complement deficiencies.

Lupus - 1 Aug 2010

Lipsker D, Hauptmann G

Abstract excerpt

In this review we address the main cutaneous manifestations and diseases associated with deficiencies in components of the complement system. The first part is devoted to hereditary angioedema, in which acute, sometimes life-threatening recurrent attacks of acute swelling, usually associated with gastrointestinal symptoms, occur. It is related to a structural or functional deficiency of C1 esterase inhibitor....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Coagulation, Bradykinin, Polyphosphates, and Angioedema
Share to Complement C2
Share to Complement C4

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Complement System Proteins

Share to Genetic Predisposition to Disease

Share to Lupus Erythematosus, Systemic

Share to Photosensitivity Disorders

Share to Skin Diseases

Source

Identifiers

PMID: 20693203
DOI: 10.1177/0961203310373370

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cutaneous manifestations of complement deficiencies.PMID 20693203Read ↗

The role of the complement system in hereditary angioedema.Semantic proximity Read ↗

Unveiling the Complexities of Hereditary Angioedema.Semantic proximity Read ↗

Hereditary Angioedema: The Clinical Picture of Excessive Contact Activation.Semantic proximity Read ↗

Hereditary and acquired angioedema.Semantic proximity Read ↗

European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management.Semantic proximity Read ↗

Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.Semantic proximity Read ↗

Hereditary Angioedema: Diagnosis, Clinical Implications, and Pathophysiology.Semantic proximity Read ↗

Systemic Lupus Erythematosus and Deficiencies of Early Components of the Complement Classical PathwaySemantic proximity Read ↗

Hereditary AngioedemaSemantic proximity Read ↗

Hereditary angioedema.Semantic proximity Read ↗

Complement disorders and hereditary angioedemaSemantic proximity Read ↗

The relevance of complement in pemphigoid diseases: A critical appraisalSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.