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Diseases » Joubert Syndrome 10 » Summary
 

What is Joubert Syndrome 10?

What is Joubert Syndrome 10?

  • Joubert Syndrome 10: Joubert syndrome is a rare congenital neurological disorder characterized mainly by a brain anomaly where the cerebellar vermis is underdeveloped. This part of the brain is responsible to for balance and coordination. Most of the symptoms are of a neurological type. There are ten subtypes of the disorder, each with a different origin for the genetic anomaly. Type 10 is linked to a defect on chromosome Xp22.3.

Joubert Syndrome 10: Introduction

Types of Joubert Syndrome 10:

Broader types of Joubert Syndrome 10:

How serious is Joubert Syndrome 10?

Prognosis of Joubert Syndrome 10: The prognosis depends mainly on how much of the cerebellar vermis portion of the brain is missing - symptoms can vary from mild to severe. Irregular breathing patterns tend to improve after about a year though apnea usually persists.
Complications of Joubert Syndrome 10: see complications of Joubert Syndrome 10

What causes Joubert Syndrome 10?

Causes of Joubert Syndrome 10: see causes of Joubert Syndrome 10

What are the symptoms of Joubert Syndrome 10?

Symptoms of Joubert Syndrome 10: see symptoms of Joubert Syndrome 10

Complications of Joubert Syndrome 10: see complications of Joubert Syndrome 10

Joubert Syndrome 10: Testing

Diagnostic testing: see tests for Joubert Syndrome 10.

Misdiagnosis: see misdiagnosis and Joubert Syndrome 10.

How is it treated?

Treatments for Joubert Syndrome 10: see treatments for Joubert Syndrome 10

Name and Aliases of Joubert Syndrome 10

Main name of condition: Joubert Syndrome 10

Other names or spellings for Joubert Syndrome 10:

JBTS10

 

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