21-Hydroxylase Deficiency history and symptoms

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21-Hydroxylase Deficiency Microchapters

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Differentiating 21-Hydroxylase Deficiency from other Diseases

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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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