Congenital Adrenal Hyperplasia (CAH) Latest Advances

Late Recognition of Aromatase Deficiency Following 16 Years of Misdiagnosis as Congenital Adrenal Hyperplasia: A Case with Coexisting Gonadoblastoma and Dysgerminoma.

Journal: Journal of clinical research in pediatric endocrinology

Published: September 01, 2026

Correction to: "Prevalence of Psychiatric Comorbidities in Females with Classic Congenital Adrenal Hyperplasia".

Journal: The Journal of clinical endocrinology and metabolism

Published: August 21, 2026

Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding.

Journal: Journal of clinical research in pediatric endocrinology

Published: August 20, 2026

A follow-up study of 10 Uyghur children with 11β-hydroxylase deficiency in the Xinjiang region

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: August 17, 2026

Congenital adrenal hyperplasia, ovarian adrenal rest tumours and Addison's disease: an exceptional clinical constellation.

Journal: BMJ case reports

Published: August 14, 2026

Crinecerfont: emerging role in the management of congenital adrenal hyperplasia.

Journal: Expert review of endocrinology & metabolism

Published: August 04, 2026

Beckwith-Wiedemann Syndrome Presenting with Transient Features of Congenital Adrenal Hyperplasia in a Nigerian Neonate.

Journal: Nigerian medical journal : journal of the Nigeria Medical Association

Published: August 03, 2026

Disparities in Congenital Adrenal Hyperplasia Screening Follow-up Times Between Immigrants/Refugees and Local Populations in Türkiye: A Cross-Sectional Study.

Journal: Turkish archives of pediatrics

Published: August 01, 2026

Timing of 17-hydroxyprogesterone measurement during the standard-dose Synacthen test in pediatric patients evaluated for non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Journal: Archives of endocrinology and metabolism

Published: July 31, 2026

Striking Scrotal Hyperpigmentation as an Early Clinical Sign of Familial Glucocorticoid Deficiency Type 2: A Case with Homozygous MRAP Variant.

Journal: Journal of clinical research in pediatric endocrinology

Published: July 22, 2026

Dried blood microsampling: a tool to mitigate the post-sampling formation of 11-ketotestosterone in blood?

Journal: Clinical chemistry and laboratory medicine

Published: July 13, 2026

Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants.

Journal: Archives of endocrinology and metabolism

Published: July 10, 2026

Congenital Adrenal Hyperplasia (CAH) Latest Advances

Find the Latest Research About Congenital Adrenal Hyperplasia (CAH)

Late Recognition of Aromatase Deficiency Following 16 Years of Misdiagnosis as Congenital Adrenal Hyperplasia: A Case with Coexisting Gonadoblastoma and Dysgerminoma.

Late Recognition of Aromatase Deficiency Following 16 Years of Misdiagnosis as Congenital Adrenal Hyperplasia: A Case with Coexisting Gonadoblastoma and Dysgerminoma.

Correction to: "Prevalence of Psychiatric Comorbidities in Females with Classic Congenital Adrenal Hyperplasia".

Correction to: "Prevalence of Psychiatric Comorbidities in Females with Classic Congenital Adrenal Hyperplasia".

Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding.

Microscopic Müllerian Duct Remnants in a 46,XY Individual with Genetically Confirmed 17α-Hydroxylase/17,20-Lyase Deficiency: an Unexpected Histopathological Finding.

A follow-up study of 10 Uyghur children with 11β-hydroxylase deficiency in the Xinjiang region

A follow-up study of 10 Uyghur children with 11β-hydroxylase deficiency in the Xinjiang region

Congenital adrenal hyperplasia, ovarian adrenal rest tumours and Addison's disease: an exceptional clinical constellation.

Congenital adrenal hyperplasia, ovarian adrenal rest tumours and Addison's disease: an exceptional clinical constellation.

Crinecerfont: emerging role in the management of congenital adrenal hyperplasia.

Crinecerfont: emerging role in the management of congenital adrenal hyperplasia.

Beckwith-Wiedemann Syndrome Presenting with Transient Features of Congenital Adrenal Hyperplasia in a Nigerian Neonate.

Beckwith-Wiedemann Syndrome Presenting with Transient Features of Congenital Adrenal Hyperplasia in a Nigerian Neonate.

Disparities in Congenital Adrenal Hyperplasia Screening Follow-up Times Between Immigrants/Refugees and Local Populations in Türkiye: A Cross-Sectional Study.

Disparities in Congenital Adrenal Hyperplasia Screening Follow-up Times Between Immigrants/Refugees and Local Populations in Türkiye: A Cross-Sectional Study.

Timing of 17-hydroxyprogesterone measurement during the standard-dose Synacthen test in pediatric patients evaluated for non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Timing of 17-hydroxyprogesterone measurement during the standard-dose Synacthen test in pediatric patients evaluated for non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Striking Scrotal Hyperpigmentation as an Early Clinical Sign of Familial Glucocorticoid Deficiency Type 2: A Case with Homozygous MRAP Variant.

Striking Scrotal Hyperpigmentation as an Early Clinical Sign of Familial Glucocorticoid Deficiency Type 2: A Case with Homozygous MRAP Variant.

Dried blood microsampling: a tool to mitigate the post-sampling formation of 11-ketotestosterone in blood?

Dried blood microsampling: a tool to mitigate the post-sampling formation of 11-ketotestosterone in blood?

Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants.

Rare types of congenital adrenal hyperplasia: report of five children with 11β-hydroxylase deficiency including pathogenic and novel CYP11B1 variants.