Copyright
©The Author(s) 2022.
World J Clin Cases. Apr 16, 2022; 10(11): 3553-3560
Published online Apr 16, 2022. doi: 10.12998/wjcc.v10.i11.3553
Published online Apr 16, 2022. doi: 10.12998/wjcc.v10.i11.3553
Figure 1 Physical examinations.
A and B: The patient showed absence of breast development and axillary hair; C and D: The patient's vulva was similar to that of a female infant and had no pubic hair.
Figure 2 Imaging examinations.
A: Plain computed tomography (CT) scan of adrenals; B: Enhanced CT scan of adrenals; C: Plain magnetic resonance imaging scan of the pituitary gland; D: X-ray examination of both hands; E: Ultrasonography of the pelvis.
Figure 3 Cytochrome P450 family 17 subfamily A member 1 gene analysis.
A: The patient; B: Her father; C: Her mother.
- Citation: Gong Y, Qin F, Li WJ, Li LY, He P, Zhou XJ. Cytochrome P450 family 17 subfamily A member 1 mutation causes severe pseudohermaphroditism: A case report. World J Clin Cases 2022; 10(11): 3553-3560
- URL: https://www.wjgnet.com/2307-8960/full/v10/i11/3553.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i11.3553