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What is Thakker-Donnai syndrome?

What is Thakker-Donnai syndrome?

  • Thakker-Donnai syndrome: A very rare, severe genetic syndrome characterized by abnormal internal organs and facial anomalies.

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

Thakker-Donnai syndrome: Introduction

Types of Thakker-Donnai syndrome:

Broader types of Thakker-Donnai syndrome:

How serious is Thakker-Donnai syndrome?

Complications of Thakker-Donnai syndrome: see complications of Thakker-Donnai syndrome

What causes Thakker-Donnai syndrome?

Causes of Thakker-Donnai syndrome: see causes of Thakker-Donnai syndrome

What are the symptoms of Thakker-Donnai syndrome?

Symptoms of Thakker-Donnai syndrome: see symptoms of Thakker-Donnai syndrome

Complications of Thakker-Donnai syndrome: see complications of Thakker-Donnai syndrome

Thakker-Donnai syndrome: Testing

Diagnostic testing: see tests for Thakker-Donnai syndrome.

Misdiagnosis: see misdiagnosis and Thakker-Donnai syndrome.

How is it treated?

Doctors and Medical Specialists for Thakker-Donnai syndrome: Pediatrician ; see also doctors and medical specialists for Thakker-Donnai syndrome.
Treatments for Thakker-Donnai syndrome: see treatments for Thakker-Donnai syndrome

Name and Aliases of Thakker-Donnai syndrome

Main name of condition: Thakker-Donnai syndrome

Other names or spellings for Thakker-Donnai syndrome:

dysmorphism [multiple structural anomalies], Dysmorphism multiple structural anomalies, Dysmorphic facial features and multiple structural abnormalities

Dysmorphic facial features and multiple structural abnormalities, Dysmorphism multiple structural anomalies
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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