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Article

Additional diverse findings expand the clinical presentation of DOCK8 deficiency.

Journal of clinical immunology - 1 Aug 2012

Sanal Ozden, Jing Huie, Ozgur Tuba, Ayvaz Deniz, Strauss-Albee Dara M, Ersoy-Evans Sibel, Tezcan Ilhan, Turkkani Gulten, Matthews Helen F, Haliloglu Goknur, Yuce Aysel, Yalcin Bilgehan, Gokoz Ozay, Oguz Kader K, Su Helen C

Abstract excerpt

We describe seven Turkish children with DOCK8 deficiency who have not been previously reported. Three patients presented with typical features of recurrent or severe cutaneous viral infections, atopic dermatitis, and recurrent respiratory or gastrointestinal tract infections. However, four patients presented with other features. Patient 1-1 featured sclerosing cholangitis and colitis; patient 2-1, granulomatous...

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Source

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Identifiers

PMID: 22476911
DOI: 10.1007/s10875-012-9664-5
PMCID: PMC3732775

Genes

DOCK8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

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Additional diverse findings expand the clinical presentation of DOCK8 deficiency.PMID 22476911Read ↗

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Clinical and molecular profile of 17 patients with DOCK8 deficiency: A single-centre experience from Southern IndiaSemantic proximity Read ↗

Recent Advances in DOCK8 Immunodeficiency Syndrome.Semantic proximity Read ↗

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