Germ cell neoplasia in situ complicating 17β-hydroxysteroid dehydrogenase type 3 deficiency

Review

Abstract: 17β-hydroxysteroid dehydrogenase type 3 (17βHSD3)deficiency is an autosomal recessive disorder of ma

Palabras claves:

17β-hydroxysteroid dehydrogenase type 3 deficiency, 46XY disorder of sex development, Mutations, Puberty, Testosterone, Virilization

Autores:

Eugster E.A., Folsom L.J., Hjaige M., Liu J., Richard J. Auchus

Fuentes:

scopus