New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T&gt;C, p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2

Immunodeficiency

A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report

BMC Med Genet.

Esmaeilzadeh H, Bordbar MR, Dastsooz H, Silawi M, Fard MAF, Adib A, Kafashan A, Tabatabaei Z, Sadeghipour F4, Faghihi MA

doi: 10.1186/s12881-018-0647-0.

Systemic Lupus Erythematosus

A case of autoimmune severe acquired von Willebrand syndrome (type 3-like)

Transfus Apher Sci.

Gavva C, Patel P, Shen YM, Frenkel E, Sarode R

doi: 10.1016/j.transci.2017.04.006.

Immunodeficiency

A Novel STAT3 Gene Mutation Related Hyper-IgE Syndrome Misdiagnosed as Hidradenitis Suppurativa

Case Reports Immunol.

Shrestha P, Sabharwal G, Ghaffari G

doi: 10.1155/2018/4860902.

Autoimmune Disease

Rituximab treatment in seronegative autoimmune autonomic neuropathy and autoimmune autonomic ganglionopathy: Case-report and literature review

J Neuroimmunol.

Bouxin M, Schvartz B, Mestrallet S, Debrumetz A, Hentzien M, Tabary T, Cohen R, Nicolas G, Bani-Sadr F

doi: 10.1016/j.jneuroim.

Sustained clinical response after single course of rituximab as first-line monotherapy in adult-onset asthma and periocular xanthogranulomas syndrome associated with IgG4-related disease: A case report

Medicine (Baltimore).

Pomponio G, Olivari D, Mattioli M, Angeletti A, Rossetti G, Goteri G, Gabrielli A

doi: 10.1097/MD.

Systemic Lupus Erythematosus

An atypical case of late-onset systemic lupus erythematosus with systemic lymphadenopathy and severe autoimmune thrombocytopenia/neutropenia mimicking malignant lymphoma

Int J Hematol.

Tamaki K, Morishima S, Nakachi S, Kitamura S, Uchibori S, Tomori S, Hanashiro T, Shimabukuro N, Tedokon I, Morichika K, Nishi Y, Tomoyose T, Karube K, Fukushima T, Masuzaki H

doi: 10.1007/s12185-016-2126-8.

Thymoma-associated multiorgan autoimmunity with exclusive gastrointestinal tract involvement: case report and review of the literature

Virchows Arch.

Slavik T, Potgieter FM, Brittain D

doi: 10.1007/s00428-018-2304-6.

Autoimmune DiseaseRheumatoid Arthritis

The coexistence of SAPHO syndrome and rheumatoid arthritis: A case report.

Medicine (Baltimore).

Xu W, Li C, Zhang W

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Immunotherapy

A severe case of neuro-Sjögren's syndrome induced by pembrolizumab

J Immunother Cancer.

Ghosn J, Vicino A, Michielin O, Coukos G, Kuntzer T, Obeid M

doi: 10.1186/s40425-018-0429-4.

Dermatology · Immunology · Rheumatology

New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C, p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2

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