Question:
What is 21-hydroxylase deficiency?
Author: H KAnswer:
It is an autosomal recessive ch6 short arm disorder It is very polymorphic (could be complete deficiency or incomplete one) if incomplete it may present during puberty not from childhood
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H K![H K](https://lh4.googleusercontent.com/-V3rEIOcuFis/AAAAAAAAAAI/AAAAAAAAAAA/AMZuucnhTzvoiq2vqvBJhe7t9kqRkO_jNw/s96-c/photo.jpg)