Hyper IgE Syndrome Latest Advances

Orbital Abscess in an Infant With STAT3 Hyper-IgE Syndrome.

Journal: Ophthalmic plastic and reconstructive surgery

Published: March 02, 2026

Recurrent severe infections in a child with STAT3-associated hyper-IgE syndrome.

Journal: JAAD case reports

Published: December 11, 2025

DOCK8 deficiency.

Journal: Current opinion in allergy and clinical immunology

Published: October 29, 2025

Case Report: Upadacitinib for SAPHO syndrome with biologics-induced paradoxical manifestation and Hyperimmunoglobulinemia E.

Journal: Frontiers in immunology

Published: October 19, 2025

A Novel Phosphoglucomutase-3 Gene Variant Causing Milder Phenotype in Two Families.

Journal: Journal of clinical immunology

Published: October 07, 2025

Case report. Job syndrome as an unusual finding in a pediatric patient

Journal: Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)

Published: October 02, 2025

Successful Use of Tralokinumab in a Pediatric Patient With STAT3 Hyper-IgE Syndrome Following Dupilumab-Associated Conjunctivitis.

Journal: International journal of dermatology

Published: September 09, 2025

Obesity and hepatic steatosis in STAT3 hyper-IgE syndrome.

Journal: The journal of allergy and clinical immunology. In practice

Published: September 04, 2025

Understanding and Managing Hyper IgE Syndromes.

Journal: ImmunoTargets and therapy

Published: September 01, 2025

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome.

Journal: Science advances

Published: August 29, 2025

STAT3 c.1915C > T variant-associated Hyper-IgE syndrome in a child: a case report.

Journal: Frontiers in pediatrics

Published: August 26, 2025

Audiovestibular Dysfunction in Hyper-IgE Syndrome: A Systematic Review of Characteristics, Pathophysiology, Diagnosis, and Management.

Journal: International journal of molecular sciences

Published: August 21, 2025

Hyper IgE Syndrome Latest Advances

Find the Latest Research About Hyper IgE Syndrome

Orbital Abscess in an Infant With STAT3 Hyper-IgE Syndrome.

Orbital Abscess in an Infant With STAT3 Hyper-IgE Syndrome.

Recurrent severe infections in a child with STAT3-associated hyper-IgE syndrome.

Recurrent severe infections in a child with STAT3-associated hyper-IgE syndrome.

DOCK8 deficiency.

DOCK8 deficiency.

Case Report: Upadacitinib for SAPHO syndrome with biologics-induced paradoxical manifestation and Hyperimmunoglobulinemia E.

Case Report: Upadacitinib for SAPHO syndrome with biologics-induced paradoxical manifestation and Hyperimmunoglobulinemia E.

A Novel Phosphoglucomutase-3 Gene Variant Causing Milder Phenotype in Two Families.

A Novel Phosphoglucomutase-3 Gene Variant Causing Milder Phenotype in Two Families.

Case report. Job syndrome as an unusual finding in a pediatric patient

Case report. Job syndrome as an unusual finding in a pediatric patient

Successful Use of Tralokinumab in a Pediatric Patient With STAT3 Hyper-IgE Syndrome Following Dupilumab-Associated Conjunctivitis.

Successful Use of Tralokinumab in a Pediatric Patient With STAT3 Hyper-IgE Syndrome Following Dupilumab-Associated Conjunctivitis.

Obesity and hepatic steatosis in STAT3 hyper-IgE syndrome.

Obesity and hepatic steatosis in STAT3 hyper-IgE syndrome.

Understanding and Managing Hyper IgE Syndromes.

Understanding and Managing Hyper IgE Syndromes.

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome.

STAT3 haploinsufficiency is associated with autosomal dominant hyper-IgE syndrome.

STAT3 c.1915C > T variant-associated Hyper-IgE syndrome in a child: a case report.

STAT3 c.1915C > T variant-associated Hyper-IgE syndrome in a child: a case report.

Audiovestibular Dysfunction in Hyper-IgE Syndrome: A Systematic Review of Characteristics, Pathophysiology, Diagnosis, and Management.

Audiovestibular Dysfunction in Hyper-IgE Syndrome: A Systematic Review of Characteristics, Pathophysiology, Diagnosis, and Management.