The Turkish Journal of Pediatrics (Oct 2020)

A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissue

  • Sezer Acar,
  • Ece Böber,
  • Mustafa Olguner,
  • Erdener Özer,
  • Ayhan Abacı,
  • Bayram Özhan,
  • Semra Gürsoy,
  • Tufan Çankaya,
  • Hüseyin Onay,
  • Ahu Paketçi,
  • İbrahim Mert Erbaş,
  • Korcan Demir

DOI
https://doi.org/10.24953/turkjped.2020.05.015
Journal volume & issue
Vol. 62, no. 5

Abstract

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Background. Aromatase deficiency leading to virilization in mother and female fetuses during pregnancy is a rare disease. It is characterized by impaired estrogen production, increased gonadotropins, and ovarian cysts. Case. Herein, we report a clinical phenotype of the virilized female due to a novel compound heterozygous variant in CYP19A1 [IVS10 + 1 G > A; c.344 G > A (p.R115Q)], with normal gonadotropin levels at the time of admission and histologically normal ovarian tissues. Conclusion. Aromatase deficiency should also be considered even if the initial follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels are normal, and ovarian cysts are lacking.

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