Pediatric Emergency Medicine Simulation: Hyperkalemia due to Congenital Adrenal Hyperplasia
Abstract Congenital adrenal hyperplasia is a group of autosomal recessive diseases marked by mutation of the genes involved in steroidogenesis. There are many types of the disease with 21-hydroxylase deficiency comprising 90-95% of cases. Medical providers must be able to identify the signs and symp...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Association of American Medical Colleges,
2015-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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