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Case Reports
. 2020 Feb;67(2):e28084.
doi: 10.1002/pbc.28084. Epub 2019 Nov 20.

Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome

Zahra Aryan  1   2   3   4 , Mohammad Nabavi  5 , Mahsima Shabani  2   4 , Sevgi Keles  6   7 , Samaneh Zoghi  4   8 , Talal Chatila  6   7 , Nima Rezaei  2   3   8
Affiliations
Case Reports

Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome

Zahra Aryan et al. Pediatr Blood Cancer. 2020 Feb.
No abstract available

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References

REFERENCES

    1. Engelhardt KR, McGhee S, Winkler S, et al. Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome. J Allergy Clin Immunol. 2009;124:1289.e4-1302.e4.
    1. Zhang Q, Davis JC, Lamborn IT, et al. Combined immunodeficiency associated with DOCK8 mutations. N Engl J Med. 2009;361:2046-2055.
    1. Grimbacher B, Holland SM, Gallin JI, et al. Hyper-IgE syndrome with recurrent infections-an autosomal dominant multisystem disorder. N Engl J Med. 1999;340:692-702.
    1. Holland SM, DeLeo FR, Elloumi HZ, et al. STAT3 mutations in the hyper-IgE syndrome. New Engl J Med. 2007;357:1608-1619.
    1. Jing H, Zhang Q, Zhang Y, et al. Somatic reversion in dedicator of cytokinesis 8 immunodeficiency modulates disease phenotype. J Allergy Clin Immunol. 2014;133:1667-1675.

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