Seventeen alpha-hydroxylase deficiency.

Abstract

Seventeen alpha-hydroxylase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia in which defects in the biosynthesis of cortisol and sex steroid result in mineralocorticoid excess, hypokalemic hypertension and sexual abnormalities such as pseudohermaphroditism in males, and sexual infantilism in females. The disease is inherited in an autosomal recessive pattern, and is caused by mutations in the gene encoding cytochrome P450c17 (CYP17), which is the single polypeptide that mediates both 17alpha-hydroxylase and 17,20-lyase activities. We report the case of a 15-year-old patient with 17OHD who had a female phenotype but male karyotype (46,XY). The diagnosis was made based on classical clinical features, biochemical data and molecular genetic study. Two mutations were identified by polymerase chain reaction amplification and sequencing, including a S106P point mutation in exon 2 and a 9-bp (GACTCTTTC) deletion from nucleotide position 1519 in exon 8 of CYP17. The first of these mutations was found in the father and the second in the mother, and both have been previously reported in Asia. The patient's hypertension and hypokalemia resolved after glucocorticoid replacement and treatment with potassium-sparing diuretics. Sex hormone replacement was prescribed for induction of sexual development and reduction of the final height. Prophylactic gonadectomy was scheduled. In summary, 17OHD should be suspected in patients with hypokalemic hypertension and lack of secondary sexual development so that appropriate therapy can be implemented.

• Authors: Siew-Lee Wong, San-Ging Shu, Chi-Ren Tsai
• Journal: Journal of the Formosan Medical Association = Taiwan yi zhi (J Formos Med Assoc) Vol. 105 Issue 2 Pg. 177-81 (Feb 2006) ISSN: 0929-6646 [Print] Singapore
• PMID: 16477341 (Publication Type: Case Reports, Journal Article)

Chemical References

• Steroid 17-alpha-Hydroxylase

Topics

• Adolescent
• Adrenal Hyperplasia, Congenital (diagnosis, drug therapy, genetics)
• Base Sequence
• Female
• Humans
• Hypertension (etiology, therapy)
• Hypokalemia (etiology, therapy)
• Mutation
• Sequence Deletion
• Steroid 17-alpha-Hydroxylase (genetics)