Lipoid congenital adrenal hyperplasia medical therapy: Difference between revisions

Jump to navigation Jump to search
(Created page with "__NOTOC__ {{Lipoid congential adrenal hyperplasia}} {{CMG}} ==Overview== ==References== {{reflist|2}} {{WH}} {{WS}} Category:Disease Category:Endocrinology")
 
 
Line 3: Line 3:
{{CMG}}
{{CMG}}
==Overview==
==Overview==
==Medical Therapy==
Management of salt-wasting crises and mineralocorticoid treatment are as for other forms of salt-wasting [[congenital adrenal hyperplasia]]: saline and [[fludrocortisone]].
Glucocorticoids can be provided at minimal replacement doses because there is no need for suppression of excessive adrenal androgens or mineralocorticoids. As with other forms of adrenal insufficiency, extra glucocorticoid is needed for stress coverage.
XX females with lipoid CAH may need estrogen replacement at or after puberty. To date, ovulation and pregnancy has not been reported even with early diagnosis and careful glucocorticoid replacement to suppress ACTH-induced lipid damage to the ovaries.
Nearly all XY children have been so undervirilized that they have been raised as girls. The testes have been uniformly nonfunctional and are removed to prevent long term neoplastic risk.
==References==
==References==
{{reflist|2}}
{{reflist|2}}

Latest revision as of 20:28, 19 September 2012

Lipoid congenital adrenal hyperplasia Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Lipoid CAH from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Lipoid congenital adrenal hyperplasia medical therapy On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Lipoid congenital adrenal hyperplasia medical therapy

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Lipoid congenital adrenal hyperplasia medical therapy

CDC on Lipoid congenital adrenal hyperplasia medical therapy

Lipoid congenital adrenal hyperplasia medical therapy in the news

Blogs on Lipoid congenital adrenal hyperplasia medical therapy

Directions to Hospitals Treating Lipoid congenital adrenal hyperplasia

Risk calculators and risk factors for Lipoid congenital adrenal hyperplasia medical therapy

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

Overview

Medical Therapy

Management of salt-wasting crises and mineralocorticoid treatment are as for other forms of salt-wasting congenital adrenal hyperplasia: saline and fludrocortisone.

Glucocorticoids can be provided at minimal replacement doses because there is no need for suppression of excessive adrenal androgens or mineralocorticoids. As with other forms of adrenal insufficiency, extra glucocorticoid is needed for stress coverage.

XX females with lipoid CAH may need estrogen replacement at or after puberty. To date, ovulation and pregnancy has not been reported even with early diagnosis and careful glucocorticoid replacement to suppress ACTH-induced lipid damage to the ovaries.

Nearly all XY children have been so undervirilized that they have been raised as girls. The testes have been uniformly nonfunctional and are removed to prevent long term neoplastic risk.

References

Template:WH Template:WS