What is FG syndrome 1?

What is FG syndrome 1?

• FG syndrome 1: A rare inherited disorder characterized by anal abnormalities, reduced muscle tone and abnormal brain development. In type 1, the genetic defect is located on chromosome Xq12-q21.31.

FG syndrome 1: Introduction

Types of FG syndrome 1:

Broader types of FG syndrome 1:

• Genetic conditions
• Muscle conditions
• Musculoskeletal conditions
• Brain conditions
• Head conditions
• Nervous system conditions
• Mental retardation conditions
• Intellectual or developmental disabilities
• Anorectal conditions
• Digestive conditions
• Congenital conditions - physical defects
• Congenital conditions
• more types...»

How serious is FG syndrome 1?

Complications of FG syndrome 1: see complications of FG syndrome 1

What causes FG syndrome 1?

Causes of FG syndrome 1: see causes of FG syndrome 1

What are the symptoms of FG syndrome 1?

Symptoms of FG syndrome 1: see symptoms of FG syndrome 1

Complications of FG syndrome 1: see complications of FG syndrome 1

FG syndrome 1: Testing

Diagnostic testing: see tests for FG syndrome 1.

Misdiagnosis: see misdiagnosis and FG syndrome 1.

How is it treated?

Doctors and Medical Specialists for FG syndrome 1: Medical Geneticist ; see also doctors and medical specialists for FG syndrome 1.
Treatments for FG syndrome 1: see treatments for FG syndrome 1

Name and Aliases of FG syndrome 1

Main name of condition: FG syndrome 1

FGS1, Opitz-Kaveggia syndrome, mental retardation, large head, imperforate anus, congenital hypotonia, partial agenesis of corpus callosum, Keller syndrome

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