21-Hydroxylase Deficiency history and symptoms: Difference between revisions

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[[Category:Endocrinology and Metabolic Disease]]
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Latest revision as of 20:10, 19 September 2012

Template:21-Hydroxylase Deficiency Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

History and Symptoms

The early symptoms are spitting and poor weight gain, but most infants with severe CAH develop vomiting, severe dehydration, and circulatory collapse (shock) by the second or third week of life.

References

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