Hyperemesis gravidarum pathophysiology

Hyperemesis gravidarum Microchapters
Home
Patient Information
Overview
Pathophysiology
Causes
Differentiating Hyperemesis gravidarum from other Diseases
Epidemiology and Demographics
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms
Physical Examination
Laboratory Findings
CT
MRI
Ultrasound
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Hyperemesis gravidarum pathophysiology On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Hyperemesis gravidarum pathophysiology All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Hyperemesis gravidarum pathophysiology
CDC on Hyperemesis gravidarum pathophysiology
Hyperemesis gravidarum pathophysiology in the news
Blogs on Hyperemesis gravidarum pathophysiology
Directions to Hospitals Treating Hyperemesis gravidarum
Risk calculators and risk factors for Hyperemesis gravidarum pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

Overview

Development of hyperemesis gravidarum is the result from multiple genetic mutations. Hyperemesis gravidarum usually develops during the 2nd trimester of pregnancy.

Genetics

• Hyperemesis gravidarum is transmitted in dominant pattern.
• Gene 1B-alpha2Y is highly associated with hyperemesis gravidarum and twin pregnancies.

Associated Conditions

The most important conditions associated with hyperemesis gravidarum include:

• Molar pregnancy
• Twins
• Down syndrome