Article
Female pseudohermaphroditism and inefficient peak bone mass in an untreated subject affected by 21-hydroxylase congenital adrenal hyperplasia.
Journal of endocrinological investigation - 1 May 2000
Valentino R, Savastano S, Tommaselli A P, Dorato M, Scarpitta M T, Calvanese E, Del Puente A, Lombardi G
Abstract excerpt
Here we describe a subject with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-CAH), in its classical virilizing form, who presented at birth ambiguous genitalia and subsequently was assigned by the parents as male. At the age of 8 years, he underwent a two-step surgical correction of hypospadia and at 22 years old, uterus and ovaries were removed and a bilateral testicular prothesis was...
Topics
- Adrenal Hyperplasia, Congenital
- Adult
- Androgens
- Bone Density
- Bone Diseases, Metabolic
- Calcium
- Diphosphonates
- Disorders of Sex Development
- Female
- Humans
- Phenotype
- Spine
- Vitamin D
