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

Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndrome.

Ocular immunology and inflammation - 1 Jan 2000

Schuster Andreas, Apfelstedt-Sylla Eckart, Pusch Carsten M, Zrenner Eberhart, Thirkill Charles E

Abstract excerpt

PURPOSE: To report the clinical, electrophysiological, and immunological features of a patient with X-linked hyper-IgM immunodeficiency syndrome type 1 (HIGM1) accompanied by a novel type of autoimmune retinopathy, including retinal pigment epithelium (RPE) hypersensitivity. METHODS: Comprehensive ophthalmological examinations, electrophysiological function testing, and inquiries into the immunological status of...

Read the complete abstract on PubMed

Topics

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

Share to Chaperonins
Share to Hypergammaglobulinemia

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

Share to Hypersensitivity

Share to Immunologic Deficiency Syndromes

Share to Pigment Epithelium of Eye

Share to Retinal Diseases

Share to Visual Acuity

Share to Visual Fields

Source

Identifiers

PMID: 16019685
DOI: 10.1080/09273940590928571

Genes

RPE
ERG

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.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndrome.PMID 16019685Read ↗

Retinopathy caused by a primary immune regulatory disorder - the spectrum of AIRE-associated retinopathy: case series and literature review.Semantic proximity Read ↗

Molecular pathology of X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1).Semantic proximity Read ↗

Immune function in X-linked retinoschisis subjects in an AAV8-RS1 phase I/IIa gene therapy trial.Semantic proximity Read ↗

Retinal degeneration in autoimmune polyglandular syndrome type 1: a case series.Semantic proximity Read ↗

Autoimmune Retinopathy Complicating TLR7-related Monogenic Interferonopathy.Semantic proximity Read ↗

Clinical, biological, electrophysiological and therapeutic profile of patients with anti-MAG neuropathy according to MYD88L265P and CXCR4 mutations and underlying haemopathy.Semantic proximity Read ↗

Clinical and pathological heterogeneity in a series of 31 patients with IgM-related neuropathy.Semantic proximity Read ↗

Characterization of neuropathies associated with elevated IgM serum levels.Semantic proximity Read ↗

Autoimmune retinopathy in a patient with autoimmune polyendocrine syndrome type I.Semantic proximity Read ↗

Immune landscape in children with X-linked retinoschisisSemantic proximity Read ↗

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