Omenn Syndrome Latest Advances

Unraveling Omenn syndrome in a newborn: A case report.

Journal: JAAD case reports

Published: January 13, 2025

Thymic and T-cell intrinsic critical roles associated with severe combined immunodeficiency and Omenn syndrome due to a heterozygous variant (G201R) in PSMB10.

Journal: The Journal of allergy and clinical immunology

Published: November 25, 2024

Desmoglein-1 Deficiency Mimicking Omenn Syndrome.

Journal: Indian journal of dermatology

Published: August 09, 2024

Successful bone marrow transplantation in a patient with Omenn syndrome, a rare variant of severe combined immunodeficiency syndrome: A case report.

Journal: Clinical case reports

Published: June 04, 2024

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

Journal: Science immunology

Published: May 24, 2024

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

Journal: Science immunology

Published: May 24, 2024

HSCT in a Patient with Cernunnos/XLF Deficiency and Omenn Syndrome.

Journal: Journal of clinical immunology

Published: May 16, 2024

Omenn Syndrome can Occur during Enzyme Therapy for Adenosine Deaminase Deficiency.

Journal: Journal of clinical immunology

Published: April 30, 2024

Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3.

Journal: Journal of clinical immunology

Published: February 11, 2024

Omenn syndrome: A rare manifestation of severe combined immunodeficiency masquerading as drug reaction with eosinophilia and systemic symptoms.

Journal: Journal of paediatrics and child health

Published: November 20, 2023

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Journal: Journal of clinical immunology

Published: October 06, 2023

Proposal of Slovenian guidelines for the diagnosis of neonatal erythroderma with a case report of Omenn syndrome.

Journal: Acta dermatovenerologica Alpina, Pannonica, et Adriatica

Published: June 27, 2023

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Unraveling Omenn syndrome in a newborn: A case report.

Unraveling Omenn syndrome in a newborn: A case report.

Thymic and T-cell intrinsic critical roles associated with severe combined immunodeficiency and Omenn syndrome due to a heterozygous variant (G201R) in PSMB10.

Thymic and T-cell intrinsic critical roles associated with severe combined immunodeficiency and Omenn syndrome due to a heterozygous variant (G201R) in PSMB10.

Desmoglein-1 Deficiency Mimicking Omenn Syndrome.

Desmoglein-1 Deficiency Mimicking Omenn Syndrome.

Successful bone marrow transplantation in a patient with Omenn syndrome, a rare variant of severe combined immunodeficiency syndrome: A case report.

Successful bone marrow transplantation in a patient with Omenn syndrome, a rare variant of severe combined immunodeficiency syndrome: A case report.

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

HSCT in a Patient with Cernunnos/XLF Deficiency and Omenn Syndrome.

HSCT in a Patient with Cernunnos/XLF Deficiency and Omenn Syndrome.

Omenn Syndrome can Occur during Enzyme Therapy for Adenosine Deaminase Deficiency.

Omenn Syndrome can Occur during Enzyme Therapy for Adenosine Deaminase Deficiency.

Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3.

Omenn Syndrome in Two Infants with Different Hypomorphic Variants in Janus Kinase 3.

Omenn syndrome: A rare manifestation of severe combined immunodeficiency masquerading as drug reaction with eosinophilia and systemic symptoms.

Omenn syndrome: A rare manifestation of severe combined immunodeficiency masquerading as drug reaction with eosinophilia and systemic symptoms.

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Proposal of Slovenian guidelines for the diagnosis of neonatal erythroderma with a case report of Omenn syndrome.

Proposal of Slovenian guidelines for the diagnosis of neonatal erythroderma with a case report of Omenn syndrome.