Familial Glucocorticoid Deficiency Latest Advances

A Case of Hypopituitarism Accompanied with Delusion: The Effects of Growth Hormone Replacement Therapy.

Journal: Internal medicine (Tokyo, Japan)

Published: August 27, 2025

Glucocorticoid resistance syndrome: A systematic review of the genotypes, phenotypes, and their relationships.

Journal: Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists

Published: July 15, 2025

The Current Treatment Landscape for Congenital Adrenal Hyperplasia.

Journal: Drugs

Published: July 14, 2025

Polymorphism of Melanocortin Receptor Genes-Association with Inflammatory Traits and Diseases.

Journal: Diseases (Basel, Switzerland)

Published: July 12, 2025

The Importance of Disease Specific Growth Charts for Children with Congenital Adrenal Hyperplasia.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 10, 2025

46,XY 17 alpha-hydroxylase/17,20 lyase deficiency with breast development: A case report and literature review.

Journal: Endocrine journal

Published: June 22, 2025

Bone Health in Youth with Congenital Adrenal Hyperplasia: Abdominal and Total Adiposity is Associated with Bone Mineral Density.

Journal: Hormone research in paediatrics

Published: June 13, 2025

How should glucocorticoid and mineralocorticoid replacement be optimised in a young patient with classic 21-hydroxylase congenital adrenal hyperplasia?

Journal: Internal medicine journal

Published: June 11, 2025

Clinical outcomes and treatment adequacy assessment in congenital adrenal hyperplasia: A Single-Center experience with Long-Term Follow-Up.

Journal: Endocrine

Published: June 06, 2025

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

Journal: Ideggyogyaszati szemle

Published: June 06, 2025

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

Journal: Ideggyogyaszati szemle

Published: June 06, 2025

The Role of MRI Findings in the Treatment of Testicular Adrenal Rest Tumors in a Child With Salt-Wasting Congenital Adrenal Hyperplasia: A Case Report.

Journal: Cureus

Published: June 03, 2025

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A Case of Hypopituitarism Accompanied with Delusion: The Effects of Growth Hormone Replacement Therapy.

A Case of Hypopituitarism Accompanied with Delusion: The Effects of Growth Hormone Replacement Therapy.

Glucocorticoid resistance syndrome: A systematic review of the genotypes, phenotypes, and their relationships.

Glucocorticoid resistance syndrome: A systematic review of the genotypes, phenotypes, and their relationships.

The Current Treatment Landscape for Congenital Adrenal Hyperplasia.

The Current Treatment Landscape for Congenital Adrenal Hyperplasia.

Polymorphism of Melanocortin Receptor Genes-Association with Inflammatory Traits and Diseases.

Polymorphism of Melanocortin Receptor Genes-Association with Inflammatory Traits and Diseases.

The Importance of Disease Specific Growth Charts for Children with Congenital Adrenal Hyperplasia.

The Importance of Disease Specific Growth Charts for Children with Congenital Adrenal Hyperplasia.

46,XY 17 alpha-hydroxylase/17,20 lyase deficiency with breast development: A case report and literature review.

46,XY 17 alpha-hydroxylase/17,20 lyase deficiency with breast development: A case report and literature review.

Bone Health in Youth with Congenital Adrenal Hyperplasia: Abdominal and Total Adiposity is Associated with Bone Mineral Density.

Bone Health in Youth with Congenital Adrenal Hyperplasia: Abdominal and Total Adiposity is Associated with Bone Mineral Density.

How should glucocorticoid and mineralocorticoid replacement be optimised in a young patient with classic 21-hydroxylase congenital adrenal hyperplasia?

How should glucocorticoid and mineralocorticoid replacement be optimised in a young patient with classic 21-hydroxylase congenital adrenal hyperplasia?

Clinical outcomes and treatment adequacy assessment in congenital adrenal hyperplasia: A Single-Center experience with Long-Term Follow-Up.

Clinical outcomes and treatment adequacy assessment in congenital adrenal hyperplasia: A Single-Center experience with Long-Term Follow-Up.

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

A triple A syndrome with neurological findings; c464G>A mutation in the AAAS gene.

The Role of MRI Findings in the Treatment of Testicular Adrenal Rest Tumors in a Child With Salt-Wasting Congenital Adrenal Hyperplasia: A Case Report.

The Role of MRI Findings in the Treatment of Testicular Adrenal Rest Tumors in a Child With Salt-Wasting Congenital Adrenal Hyperplasia: A Case Report.