Pseudohypoaldosteronism Type 2 Latest Advances

Long-Term Immune Alterations After Thymectomy in Early Childhood: A Case Series.

Journal: Cureus

Published: October 27, 2025

Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis.

Journal: European journal of case reports in internal medicine

Published: September 26, 2025

Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: September 16, 2025

Cardiac arrest in a previously healthy infant caused by secondary pseudohypoaldosteronism: Case report and literature review.

Journal: Medicina intensiva

Published: August 13, 2025

Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia.

Journal: Cureus

Published: August 03, 2025

A case report of Graves' disease combined with pseudohypoaldosteronism type IID in a child.

Journal: Translational pediatrics

Published: July 24, 2025

Repeated pseudohypoaldosteronism (PHA1) in pregnancy associated with fetal growth restriction: case report and review of the literature.

Journal: BMC pregnancy and childbirth

Published: July 12, 2025

A Case of Secondary Pseudohypoaldosteronism in a Neonate not Due to Urinary Tract Issues.

Journal: Journal of clinical research in pediatric endocrinology

Published: July 11, 2025

The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 01, 2025

Pseudo-Hypoaldosteronism Type 2 due to New Variants of KLHL3 Gene Diagnosed in an Adult Woman With Very High Sensitivity to Hydrochlorothiazide.

Journal: Clinical case reports

Published: June 30, 2025

Prenatal Diagnosis of Autosomal Dominant Pseudohypoaldosteronism due to NR3C2 Gene Mutation: Immediate Postnatal Oral Saline Therapy Prevents the Clinical Manifestations Resulting from Impaired Salt Balance.

Journal: Hormone research in paediatrics

Published: June 29, 2025

Three cases of pseudohypoaldosteronism type Ⅱ

Journal: Zhonghua xin xue guan bing za zhi

Published: June 18, 2025

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Long-Term Immune Alterations After Thymectomy in Early Childhood: A Case Series.

Long-Term Immune Alterations After Thymectomy in Early Childhood: A Case Series.

Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis.

Pseudohypoaldosteronism type II: The Relevance of A Challenging Diagnosis.

Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2.

Diagnostic pitfalls in aldosterone defects: a 9-year follow-up of early-onset pseudohypoaldosteronism type 2.

Cardiac arrest in a previously healthy infant caused by secondary pseudohypoaldosteronism: Case report and literature review.

Cardiac arrest in a previously healthy infant caused by secondary pseudohypoaldosteronism: Case report and literature review.

Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia.

Life-Threatening Hyponatremia, Hyperkalemia, and Shock in Infancy: Not Always Congenital Adrenal Hyperplasia.

A case report of Graves' disease combined with pseudohypoaldosteronism type IID in a child.

A case report of Graves' disease combined with pseudohypoaldosteronism type IID in a child.

Repeated pseudohypoaldosteronism (PHA1) in pregnancy associated with fetal growth restriction: case report and review of the literature.

Repeated pseudohypoaldosteronism (PHA1) in pregnancy associated with fetal growth restriction: case report and review of the literature.

A Case of Secondary Pseudohypoaldosteronism in a Neonate not Due to Urinary Tract Issues.

A Case of Secondary Pseudohypoaldosteronism in a Neonate not Due to Urinary Tract Issues.

The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.

The first report of a gross deletion in the SCNN1G gene in a case presenting with hyponatremic convulsion at fifth year of treatment.

Pseudo-Hypoaldosteronism Type 2 due to New Variants of KLHL3 Gene Diagnosed in an Adult Woman With Very High Sensitivity to Hydrochlorothiazide.

Pseudo-Hypoaldosteronism Type 2 due to New Variants of KLHL3 Gene Diagnosed in an Adult Woman With Very High Sensitivity to Hydrochlorothiazide.

Prenatal Diagnosis of Autosomal Dominant Pseudohypoaldosteronism due to NR3C2 Gene Mutation: Immediate Postnatal Oral Saline Therapy Prevents the Clinical Manifestations Resulting from Impaired Salt Balance.

Prenatal Diagnosis of Autosomal Dominant Pseudohypoaldosteronism due to NR3C2 Gene Mutation: Immediate Postnatal Oral Saline Therapy Prevents the Clinical Manifestations Resulting from Impaired Salt Balance.

Three cases of pseudohypoaldosteronism type Ⅱ

Three cases of pseudohypoaldosteronism type Ⅱ