Lipoid congenital adrenal hyperplasia epidemiology and demographics: Difference between revisions

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==Overview==
==Epidemiology and Demographics==
Lipoid CAH is quite rare in European and North American populations. Most cases have occurred in Japan and Korea (where the incidence is 1 in 300,000 births) and Palestinian Arabs. Despite autosomal recessive inheritance, there has been an unexplained preponderance of genetic females in reported cases
Lipoid CAH is quite rare in European and North American populations. Most cases have occurred in Japan and Korea (where the incidence is 1 in 300,000 births) and Palestinian Arabs. Despite autosomal recessive inheritance, there has been an unexplained preponderance of genetic females in reported cases
==References==
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[[Category:Disease]]
[[Category:Endocrinology]]

Latest revision as of 20:29, 19 September 2012

Lipoid congenital adrenal hyperplasia Microchapters

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Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Lipoid CAH from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

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Laboratory Findings

Electrocardiogram

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

Overview

Epidemiology and Demographics

Lipoid CAH is quite rare in European and North American populations. Most cases have occurred in Japan and Korea (where the incidence is 1 in 300,000 births) and Palestinian Arabs. Despite autosomal recessive inheritance, there has been an unexplained preponderance of genetic females in reported cases

References

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