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What is Madokoro-Ohdo-Sonoda syndrome?

What is Madokoro-Ohdo-Sonoda syndrome?

  • Madokoro-Ohdo-Sonoda syndrome: A rare disorder characterized by the absence of all four limbs, an unusual face and retarded development.

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

Madokoro-Ohdo-Sonoda syndrome: Introduction

Types of Madokoro-Ohdo-Sonoda syndrome:

Broader types of Madokoro-Ohdo-Sonoda syndrome:

What causes Madokoro-Ohdo-Sonoda syndrome?

Causes of Madokoro-Ohdo-Sonoda syndrome: see causes of Madokoro-Ohdo-Sonoda syndrome

What are the symptoms of Madokoro-Ohdo-Sonoda syndrome?

Symptoms of Madokoro-Ohdo-Sonoda syndrome: see symptoms of Madokoro-Ohdo-Sonoda syndrome

Madokoro-Ohdo-Sonoda syndrome: Testing

Diagnostic testing: see tests for Madokoro-Ohdo-Sonoda syndrome.

Misdiagnosis: see misdiagnosis and Madokoro-Ohdo-Sonoda syndrome.

How is it treated?

Doctors and Medical Specialists for Madokoro-Ohdo-Sonoda syndrome: Neonatologist ; see also doctors and medical specialists for Madokoro-Ohdo-Sonoda syndrome.
Treatments for Madokoro-Ohdo-Sonoda syndrome: see treatments for Madokoro-Ohdo-Sonoda syndrome

Name and Aliases of Madokoro-Ohdo-Sonoda syndrome

Main name of condition: Madokoro-Ohdo-Sonoda syndrome

Other names or spellings for Madokoro-Ohdo-Sonoda syndrome:

tetra-amelia with ectodermal dysplasia and lacrimal duct abnormalities, Tetra-amelia, ectodermal dysplasia, and lacrimal duct abnormality

Association of tetra-amelia, ectodermal dysplasia, hypoplastic lacrimal ducts and sacs opening towards the exterior, peculiar face, and developmental
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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