Hyper-IgE syndrome caused by DOCK8 mutation with a tumour-like lesion of the lip: a case report-Reference-Cited by-同舟云学术

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Hyper-IgE syndrome caused by DOCK8 mutation with a tumour-like lesion of the lip: a case report

Published:2022-12 Issue:12 Volume:51 Page:1545-1548
ISSN:0901-5027
Container-title:International Journal of Oral and Maxillofacial Surgery
language:en
Short-container-title:International Journal of Oral and Maxillofacial Surgery

Author:

Zhu W.-X.,Liu Y.-Y.,Hua H.,Yu G.-Y.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,Oral Surgery,Surgery

Reference12 articles.

1. Job syndrome. StatPearls. Treasure Island;Hafsi,2021

2. Hyper IgE (Job’s) syndrome: a primary immune deficiency with oral manifestations;Freeman;Oral Dis,2009

3. Autosomal recessive hyper-IgE syndrome caused by DOCK8 gene mutation with new clinical features: a case report;Yang;BMC Neurol,2021

4. Insights into immunity from clinical and basic science studies of DOCK8 immunodeficiency syndrome;Su;Immunol Rev,2019

5. DOCK8 deficiency: clinical and immunological phenotype and treatment options—a review of 136 patients;Aydin;J Clin Immunol,2015

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