A female pseudohermaphrodite with salt losing congenital adrenal hyperplasia as the result of 21 β OH deficiency
A type 4, female pseudohermaphrodite due to virilizing congenital adrenal hyperplasia resulting from 21 β hydroxylase deficiency was reported. Salt losing manifestations developed within the first month of life. The salt losing adrenal insufficiency was well controlled by glucocorticoid, mineralocor...
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| Main Authors: | , , , |
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| Other Authors: | |
| Format: | Article |
| Published: |
2018
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| Subjects: | |
| Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/10815 |
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| Institution: | Mahidol University |