Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia*

@inproceedings{Kohn1982LateOnsetS2,
  title={Late-Onset Steroid 21-Hydroxylase Deficiency: A Variant of Classical Congenital Adrenal Hyperplasia*},
  author={B Kohn and Lenore Levine and Marilyn S. Pollack and Songya Pang and Franziska Lorenzen and D Levy and Alan J. Lerner and G. F. Rondanini and Bo Dupont and Maria I. New},
  year={1982}
}
Hormonal studies and human leukocyte antigen (HLA) genotyping were performed in 5 males and 13 females who were demonstrated to have 21-hydroxylase deficiency. The enzymatic deficiency of steroidogenesis was detected by family studies of 10 females who presented with varying symptoms of androgen excess. The 10 index cases had normal genitalia at birth, but virilized to varying degrees postnatally. The additional 8 affected family members had not sought medical care, but some were found to have… CONTINUE READING

Citations

Publications citing this paper.
SHOWING 1-10 OF 31 CITATIONS

Non-Classical Congenital Adrenal Hyperplasia in Childhood

  • Journal of clinical research in pediatric endocrinology
  • 2017
VIEW 1 EXCERPT
CITES METHODS

Differential diagnosis of hyperandrogenism in women with polycystic ovary syndrome.

  • Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association
  • 2012