21 Hydroxylase Deficiency - Gynecology

Relevant Publications

Phase 3 Trial of Crinecerfont in Adult Congenital Adrenal Hyperplasia.

Issue Release: 2024

A Rare Case of Giant Bilateral Adrenal Myelolipomas in a Patient With Classical Congenital Hyperplasia.

Issue Release: 2024

Severe adrenal insufficiency in six neonates with normal newborn screening for CAH.

Issue Release: 2024

Severe Carpal Tunnel Syndrome in a Pediatric Patient With a History of Congenital Adrenal Hyperplasia.

Issue Release: 2024

Biochemical monitoring of 21-hydroxylase deficiency: a clinical utility of overnight fasting urine pregnanetriol.

Issue Release: 2024

A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia--R484Q Mutant Mouse.

Issue Release: 2024

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening.

Issue Release: 2024

Giant Bilateral Adrenal Myelolipomas in a Non-Compliant Patient with Congenital Adrenal Hyperplasia.

Issue Release: 2024

Parental concerns about genital differences in children with congenital adrenal hyperplasia persist regardless of the selected intervention.

Issue Release: 2024

Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene.

Issue Release: 2024

Landscape of congenital adrenal hyperplasia cases in adult endocrinology clinics of Türkiye-a nation-wide multicentre study.

Issue Release: 2024

Genotype and Phenotype of 21-Hydroxylase Deficiency: A Single Center Experience from Western India.

Issue Release: 2024

46,XX males with congenital adrenal hyperplasia: a clinical and biochemical description.

Issue Release: 2024

Free cortisol and free 21-deoxycortisol in the clinical evaluation of congenital adrenal hyperplasia.

Issue Release: 2024

Neural Correlates of Obesity and Inflammation in Children and Adolescents with Congenital Adrenal Hyperplasia.

Issue Release: 2024

Rare nonclassic type of Congenital adrenal hyperplasia due to 21-hydroxylase deficiency and genotype-phenotypic correlation.

Issue Release: 2024

Alkindi Sprinkle for Pediatric Patients With Primary Adrenocortical Insufficiency: A Narrative Review.

Issue Release: 2024

Dual rare genetic diseases in five pediatric patients: insights from next-generation diagnostic methods.

Issue Release: 2024

Case report: Development of central precocious puberty in a girl with late-diagnosed simple virilizing congenital adrenal hyperplasia complicated with Williams syndrome.

Issue Release: 2024

Challenging Molecular Diagnosis of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency: Case Series and Novel Variants of Gene.

Issue Release: 2024

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