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

Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection

21 Oct 2016

Abstract excerpt

EBNA Epstein-Barr nuclear antigenTo the Editor Kaposi sarcoma (KS) in children is rare and generally associated with loss of CD4+ T cells in human immunodeficiency virus (HIV) infected patients and impaired immunity to human herpes virus 8 (HHV-8), or is caused by specific singlegene inborn errors in IFNGR1, WAS, STIM1, and OX40 genes, that apparently confer selective protective immunity against Alessandro Aiuti...

Read the complete abstract on PubMed

Topics

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

Share to Histiocytic Disorders and Treatments
Share to Parvovirus B19 Infection Studies
Share to Viral-associated cancers and disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 27770395
DOI: 10.1007/s10875-016-0341-y

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

Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV InfectionPMID 27770395Read ↗

MAGT1 gene mutation causes myositis and CD127 expression downregulationSemantic proximity Read ↗

Inherited Immunodeficiencies With High Predisposition to Epstein-Barr Virus-Driven Lymphoproliferative Diseases.Semantic proximity Read ↗

Scales of Magt1 Gene: Novel Mutations, Different Presentations.Semantic proximity Read ↗

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma.Semantic proximity Read ↗

Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN diseaseSemantic proximity Read ↗

XMEN-associated Systemic EBV-positive T-cell Lymphoma of Childhood: Report of Two Cases and Literature Review.Semantic proximity Read ↗

Not enough by half: NFAT5 haploinsufficiency in two patients with Epstein-Barr virus susceptibilitySemantic proximity Read ↗

Evaluation of T Cell Repertoire in Primary Immunodeficiencies With Dna Repair DefectsSemantic proximity Read ↗

Modifier-Sensitive Phenotypic Divergence in XMEN Disease (MAGT1 Deficiency): Neurodegenerative and Hematologic TrajectoriesSemantic proximity Read ↗

Epidermodysplasia Verruciformis and Vδ2 γδ T-cell Expansion in STK4 Deficiency.Semantic proximity Read ↗

Ataxia Telangiectasia Diagnosed on Newborn Screening-Case Cohort of 5 Years' Experience.Semantic proximity Read ↗

Autoimmune cytopenia and Kabuki syndrome in paediatrics: Insights in 11 patients.Semantic proximity Read ↗

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