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Revision as of 04:58, 20 September 2012

Autoimmune polyendocrine syndrome
ICD-10 E31.0
ICD-9 258.1
OMIM 240300 269200
DiseasesDB 29212 Template:DiseasesDB2

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

Overview

Classification

The polyendocrine deficiency syndrome is classified into two separate forms, referred to as type I and type II.

Type I occurs in children, and adrenal insufficiency may be accompanied by:

Type II, often called Schmidt's syndrome, usually afflicts young adults. Features of type II may include:

Scientists think that the polyendocrine deficiency syndrome is inherited because frequently more than one family member tends to have one or more endocrine deficiencies.

References

Related Chapters


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