Growth hormone deficiency overview: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
Line 8: Line 8:
Other hormonal or glandular disorders frequently coincide with diminished growth hormone production. GH deficiency can be congenital or acquired in childhood or adult life. It can be partial or complete. It is usually permanent, but sometimes transient. It may be an isolated deficiency or occur in association with deficiencies of other [[pituitary]] hormones. GH deficiency is treated by [[growth hormone treatment|growth hormone replacement]].
Other hormonal or glandular disorders frequently coincide with diminished growth hormone production. GH deficiency can be congenital or acquired in childhood or adult life. It can be partial or complete. It is usually permanent, but sometimes transient. It may be an isolated deficiency or occur in association with deficiencies of other [[pituitary]] hormones. GH deficiency is treated by [[growth hormone treatment|growth hormone replacement]].


The term [[hypopituitarism]] is often used interchangeably with GH deficiency by [[endocrinologist]]s but more often denotes GH deficiency plus deficiency of at least one other anterior pituitary hormone. When GH deficiency (usually with other anterior pituitary deficiencies) is associated with posterior pituitary hormone deficiency (usually [[diabetes insipidus]]) the condition is termed [[panhypopituitarism]]. HGH also refers to [[human growth hormone]] but this older abbreviation has begun to develop paradoxical connotations (see fuller discussion of HGH in [[growth hormone treatment|GH treatment]] and [[HGH quackery]]).
The term [[hypopituitarism]] is often used interchangeably with GH deficiency by [[endocrinologist]]s but more often denotes GH deficiency plus deficiency of at least one other anterior pituitary hormone. When GH deficiency (usually with other anterior pituitary deficiencies) is associated with posterior pituitary hormone deficiency (usually [[diabetes insipidus]]) the condition is termed [[panhypopituitarism]]. HGH also refers to [[human growth hormone]] but this older abbreviation has begun to develop paradoxical connotations.


==References==
==References==

Revision as of 14:45, 19 September 2012

Growth hormone deficiency Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Growth hormone deficiency from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Criteria

History and Symptoms

Physical Examination

Laboratory Findings

X Ray

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

Growth hormone deficiency overview On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Growth hormone deficiency overview

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Growth hormone deficiency overview

CDC on Growth hormone deficiency overview

Growth hormone deficiency overview in the news

Blogs on Growth hormone deficiency overview

Directions to Hospitals Treating Growth hormone deficiency

Risk calculators and risk factors for Growth hormone deficiency overview

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

Overview

Growth Hormone Deficiency is the medical condition of inadequate production of growth hormone (GH) and its effects on children and adults. Growth hormone, also called somatotropin, is a polypeptide hormone which stimulates growth and cell reproduction.

Other hormonal or glandular disorders frequently coincide with diminished growth hormone production. GH deficiency can be congenital or acquired in childhood or adult life. It can be partial or complete. It is usually permanent, but sometimes transient. It may be an isolated deficiency or occur in association with deficiencies of other pituitary hormones. GH deficiency is treated by growth hormone replacement.

The term hypopituitarism is often used interchangeably with GH deficiency by endocrinologists but more often denotes GH deficiency plus deficiency of at least one other anterior pituitary hormone. When GH deficiency (usually with other anterior pituitary deficiencies) is associated with posterior pituitary hormone deficiency (usually diabetes insipidus) the condition is termed panhypopituitarism. HGH also refers to human growth hormone but this older abbreviation has begun to develop paradoxical connotations.

References

Template:WH Template:WS