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

Chronic immune thrombocytopenia in a child with X-linked agammaglobulinemia-an uncommon phenotype.

Platelets - 3 Oct 2022

Yin Jing, Ma Jijun, Liu Xiaoxue, Xia Jingyue, Ai Qi, Li Chongwei

Abstract excerpt

Autoimmune disorders are common in patients with primary immunodeficiency diseases (PIDs). However, the prevalence of autoimmunity is low in patients with X-linked agammaglobulinemia (XLA), mostly due to the absence of antibodies. Chronic or persistent immune thrombocytopenia (ITP), which is usually considered an antibody-mediated disease, is uncommon in patients with XLA. In this study, we detailly described a...

Read the complete abstract on PubMed

Topics

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

Share to Agammaglobulinemia
Share to Autoimmunity
Share to Genetic Diseases, X-Linked

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Phenotype

Share to Purpura, Thrombocytopenic, Idiopathic

Source

Identifiers

PMID: 35296220
DOI: 10.1080/09537104.2022.2053090

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Chronic immune thrombocytopenia in a child with X-linked agammaglobulinemia-an uncommon phenotype.PMID 35296220Read ↗

T Cell Abnormalities in X-Linked Agammaglobulinaemia: an Updated Review.Semantic proximity Read ↗

A child with X-linked agammaglobulinemia and Kawasaki disease: an unusual association.Semantic proximity Read ↗

[Clinical features of X-linked agammaglobulinemia: analysis of 8 cases].Semantic proximity Read ↗

Autosomal recessive chronic granulomatous disease, IgA deficiency and refractory autoimmune thrombocytopenia responding to Anti-CD20 monoclonal antibody.Semantic proximity Read ↗

Pediatric Refractory Immune Thrombocytopenia: a Systematic ReviewSemantic proximity Read ↗

Gastrointestinal Manifestations in X-linked Agammaglobulinemia.Semantic proximity Read ↗

A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease.Semantic proximity Read ↗

X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.Semantic proximity Read ↗

Severe neutropenia in Japanese patients with x-linked agammaglobulinemia.Semantic proximity Read ↗

Unusual Polyclonal IgM in an IgG Deficient Patient with Autoimmune Lymphoproliferative Syndrome: A Case Study and Literature Review.Semantic proximity Read ↗

Retrospective study of 98 patients with X-linked agammaglobulinemia complicated with arthritis.Semantic proximity Read ↗

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).Semantic proximity Read ↗

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