Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Acromegaly

S Ezzat1

  • 1University of Toronto, Wellesley Hospital, Ontario, Canada.

Endocrinology and Metabolism Clinics of North America
|January 16, 1998
PubMed
Summary
This summary is machine-generated.

Acromegaly is a serious condition often diagnosed late, leading to long-term health issues. Recent advancements improve the diagnosis and monitoring of acromegaly patients, aiming for earlier detection and better management.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Correction: CEACAM1 impedes thyroid cancer growth but promotes invasiveness: a putative mechanism for early metastases.

Oncogene·2023
Same author

A primer on the genetics of medullary thyroid cancer.

Current oncology (Toronto, Ont.)·2020
Same author

Diagnosis and pathologic characteristics of medullary thyroid carcinoma-review of current guidelines.

Current oncology (Toronto, Ont.)·2019
Same author

From pituitary adenoma to pituitary neuroendocrine tumor (PitNET): an International Pituitary Pathology Club proposal.

Endocrine-related cancer·2017
Same author

Gonadotrope Tumors.

Progress in molecular biology and translational science·2016
Same author

Clinicopathological variations in cushing's syndrome.

Endocrine pathology·2016
Same journal

Navigating Adrenal Disease: A Comprehensive, Practical Guide for the Clinician.

Endocrinology and metabolism clinics of North America·2026
Same journal

Adrenal Disorders in Pregnancy.

Endocrinology and metabolism clinics of North America·2026
Same journal

Diagnosis and Management of Adrenocortical Carcinoma.

Endocrinology and metabolism clinics of North America·2026
Same journal

Pheochromocytomas and Paragangliomas.

Endocrinology and metabolism clinics of North America·2026
Same journal

Hereditary Conditions Associated with Adrenocortical Carcinoma, Pheochromocytoma, and Other Adrenal Tumors: Genetic Testing and Management Recommendations.

Endocrinology and metabolism clinics of North America·2026
Same journal

Primary Bilateral Macronodular Adrenal Hyperplasia.

Endocrinology and metabolism clinics of North America·2026
See all related articles

Area of Science:

  • Endocrinology
  • Internal Medicine

Background:

  • Acromegaly is a chronic, debilitating endocrine disorder caused by excess growth hormone.
  • Delayed diagnosis is common, leading to significant morbidity and delayed treatment.

Purpose of the Study:

  • To review recent advances in understanding acromegaly.
  • To evaluate the impact of current diagnostic and monitoring strategies.

Main Methods:

  • Literature review of recent studies on acromegaly.
  • Analysis of diagnostic criteria and monitoring guidelines.
  • Discussion of novel therapeutic approaches.

Main Results:

  • Acromegaly diagnosis is frequently delayed due to nonspecific symptoms.
  • Current diagnostic tools and monitoring protocols are evolving.

Related Experiment Videos

  • Advances in understanding disease mechanisms inform better patient management.
  • Conclusions:

    • Early diagnosis and effective monitoring are crucial for managing acromegaly.
    • Ongoing research continues to refine acromegaly care pathways.
    • Improved strategies can mitigate the debilitating effects of acromegaly.