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Diseases » FG Syndrome » Introduction
 

FG Syndrome

FG Syndrome: Introduction

FG Syndrome: A rare genetic disorder characterized by anal abnormalities, reduced muscle tone and a prominent forehead. More detailed information about the symptoms, causes, and treatments of FG Syndrome is available below.

Symptoms of FG Syndrome

See full list of 46 symptoms of FG Syndrome

Wrongly Diagnosed with FG Syndrome?

Videos for FG Syndrome

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See full list of 4 related videos

FG Syndrome: Related Patient Stories

FG Syndrome: Complications

Review possible medical complications related to FG Syndrome:

Causes of FG Syndrome

Read more about causes of FG Syndrome.

Disease Topics Related To FG Syndrome

Research the causes of these diseases that are similar to, or related to, FG Syndrome:

Medical Textbooks Online about FG Syndrome

Medical Books Excerpts
  • Hypotonia
  • "In A Page: Pediatric Signs and Symptoms" (2007)
 

Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.

Less Common Symptoms of FG Syndrome

See full list of 17 occasional symptoms of FG Syndrome

Evidence Based Medicine Research for FG Syndrome

Medical research articles related to FG Syndrome include:

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

Reseach about FG Syndrome

Visit our research pages for current research about FG Syndrome treatments.

User Interactive Forums

Read about other experiences, ask a question about FG Syndrome, or answer someone else's question, on our message boards:

Definitions of FG Syndrome:

A multiple congenital anomaly/mental retardation syndrome characterized by a short stature, large head, hypotonia with or without joint contractures, seizures, imperforate anus, agenesis of the corpus callosum, and characteristic facies. "FG" stands for the surnames of patients in whom the syndrome was first reported. - (Source - Diseases Database)

FG Syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that FG Syndrome, or a subtype of FG 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 FG Syndrome as a "rare disease".
Source - Orphanet


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