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What is Robinow syndrome, autosomal recessive?

What is Robinow syndrome, autosomal recessive?

  • Robinow syndrome, autosomal recessive: A rare genetic disorder characterized by a flat face, short forearms, vertebral anomalies and hypoplastic genitalia.

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

Robinow syndrome, autosomal recessive: Introduction

Types of Robinow syndrome, autosomal recessive:

Broader types of Robinow syndrome, autosomal recessive:

How serious is Robinow syndrome, autosomal recessive?

Complications of Robinow syndrome, autosomal recessive: see complications of Robinow syndrome, autosomal recessive

What causes Robinow syndrome, autosomal recessive?

Causes of Robinow syndrome, autosomal recessive: see causes of Robinow syndrome, autosomal recessive

What are the symptoms of Robinow syndrome, autosomal recessive?

Symptoms of Robinow syndrome, autosomal recessive: see symptoms of Robinow syndrome, autosomal recessive

Complications of Robinow syndrome, autosomal recessive: see complications of Robinow syndrome, autosomal recessive

Robinow syndrome, autosomal recessive: Testing

Diagnostic testing: see tests for Robinow syndrome, autosomal recessive.

Misdiagnosis: see misdiagnosis and Robinow syndrome, autosomal recessive.

How is it treated?

Doctors and Medical Specialists for Robinow syndrome, autosomal recessive: Medical Geneticist ; see also doctors and medical specialists for Robinow syndrome, autosomal recessive.
Treatments for Robinow syndrome, autosomal recessive: see treatments for Robinow syndrome, autosomal recessive

Name and Aliases of Robinow syndrome, autosomal recessive

Main name of condition: Robinow syndrome, autosomal recessive

Other names or spellings for Robinow syndrome, autosomal recessive:

Costovertebral segmentation defect - mesomelia, COVESDEM syndrome, costovertebral segmentation defect [mesomelia], Covesdem syndrome (formerly), Costovertebral segmentation defect with mesomelia (formerly)

Saal Greenstein syndrome, Robinow like syndrome, Autosomal recessive Robinow-like syndrome, Costovertebral segmentation defect with mesomelia (formerly called), Covesdem syndrome (formerly called)
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Robinow syndrome, autosomal recessive: Related Conditions

Research the causes of these diseases that are similar to, or related to, Robinow syndrome, autosomal recessive:

 

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