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Diseases » HARD syndrome » Summary
 

What is HARD syndrome?

What is HARD syndrome?

  • HARD syndrome: A rare genetic disorder characterized by a smooth brain surface and eye, genitourinary and other abnormalities.

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

HARD syndrome: Introduction

Types of HARD syndrome:

Broader types of HARD syndrome:

How serious is HARD syndrome?

Complications of HARD syndrome: see complications of HARD syndrome

What causes HARD syndrome?

Causes of HARD syndrome: see causes of HARD syndrome

What are the symptoms of HARD syndrome?

Symptoms of HARD syndrome: see symptoms of HARD syndrome

Complications of HARD syndrome: see complications of HARD syndrome

Can anyone else get HARD syndrome?

More information: see contagiousness of HARD syndrome
Inheritance: see inheritance of HARD syndrome

HARD syndrome: Testing

Diagnostic testing: see tests for HARD syndrome.

Misdiagnosis: see misdiagnosis and HARD syndrome.

How is it treated?

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

Name and Aliases of HARD syndrome

Main name of condition: HARD syndrome

Other names or spellings for HARD syndrome:

Walker-Warburg syndrome, Warburg syndrome, Chemke syndrome, Hard +/- E syndrome, COD (cerebroocular dysgenesis), Hydrocephalus [Agyria - Retinal Dysplasia - Encephalus]

COD (cerebroocular dysgenesis), Chemke syndrome, Hard +/- E syndrome, Walker-Warburg syndrome, Warburg syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

HARD syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, HARD syndrome:

 

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