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Rabson-Mendenhall syndrome

Rabson-Mendenhall syndrome: Introduction

Rabson-Mendenhall syndrome: A very rare genetic disorder involving severe insulin resistance which is where the body fails to be able to use insulin which is needed to control blood sugar levels. More detailed information about the symptoms, causes, and treatments of Rabson-Mendenhall syndrome is available below.

Symptoms of Rabson-Mendenhall syndrome

Rabson-Mendenhall syndrome: Related Patient Stories

Rabson-Mendenhall syndrome: Complications

Read more about complications of Rabson-Mendenhall syndrome.

Causes of Rabson-Mendenhall syndrome

Read more about causes of Rabson-Mendenhall syndrome.

Disease Topics Related To Rabson-Mendenhall syndrome

Research the causes of these diseases that are similar to, or related to, Rabson-Mendenhall syndrome:

Less Common Symptoms of Rabson-Mendenhall syndrome

Evidence Based Medicine Research for Rabson-Mendenhall syndrome

Medical research articles related to Rabson-Mendenhall syndrome include:

Click here to find more evidence-based articles on the TRIP Database

Research about Rabson-Mendenhall syndrome

Visit our research pages for current research about Rabson-Mendenhall syndrome treatments.

Statistics for Rabson-Mendenhall syndrome

Rabson-Mendenhall syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Rabson-Mendenhall syndrome, or answer someone else's question, on our message boards:

Definitions of Rabson-Mendenhall syndrome:

Rabson-Mendenhall syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Rabson-Mendenhall syndrome, or a subtype of Rabson-Mendenhall syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Rabson-Mendenhall syndrome as a "rare disease".
Source - Orphanet


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