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

Immune Thrombocytopenic Purpura (ITP) and Chorioretinopathy in Chronic Granulomatous Disease: A Case Report.

Journal of clinical immunology - 18 May 2024

Khanmohammadi Shaghayegh, Rezaei Nazila, Kompani Farzad, Delkhah Mona

Abstract excerpt

BACKGROUND: Chronic Granulomatous Disease (CGD) is a rare immunodeficiency disorder characterized by impaired phagocytic function, leading to recurrent infections and granuloma formation. Genetic mutations in NADPH oxidase complex components, such as CYBB, NCF1, NCF2, and CYBA genes, contribute to the pathogenesis. This case report explores the possible ocular and hematologic complications associated with CGD....

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Exome Sequencing
Share to Granulomatous Disease, Chronic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to NADPH Oxidases

Share to Purpura, Thrombocytopenic, Idiopathic

Source

Identifiers

PMID: 38760640
DOI: 10.1007/s10875-024-01731-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Immune Thrombocytopenic Purpura (ITP) and Chorioretinopathy in Chronic Granulomatous Disease: A Case Report.PMID 38760640Read ↗

Ocular manifestations in chronic granulomatous disease in Saudi Arabia.Semantic proximity Read ↗

First review of chronic granulomatous disease in Palestine: clinical and genetic characteristics.Semantic proximity Read ↗

Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece.Semantic proximity Read ↗

Geographic Variability and Pathogen-Specific Considerations in the Diagnosis and Management of Chronic Granulomatous DiseaseSemantic proximity Read ↗

Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience.Semantic proximity Read ↗

Clinical Features and Genetic Analysis of 48 Patients with Chronic Granulomatous Disease in a Single Center Study from Shanghai, China (2005-2015): New Studies and a Literature Review.Semantic proximity Read ↗

Considerations in the Diagnosis of Chronic Granulomatous Disease.Semantic proximity Read ↗

Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience.Semantic proximity Read ↗

Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families.Semantic proximity Read ↗

Chronic Granulomatous Disease: Epidemiology, Pathophysiology, and Genetic Basis of Disease.Semantic proximity Read ↗

Utility of Immunohistochemistry and Immunofluorescence in Determining the Pathogenic Variants of Chronic Granulomatous Disease.Semantic proximity Read ↗

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).Semantic proximity Read ↗

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