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What is Robinow syndrome, recessive form?

What is Robinow syndrome, recessive form?

  • Robinow syndrome, recessive form: A rare genetic disorder characterized by a flat face, short forearms, vertebral anomalies and underdeveloped genitals.

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Robinow syndrome, recessive form as a "rare disease".
Source - Orphanet

Robinow syndrome, recessive form: Introduction

Types of Robinow syndrome, recessive form:

Broader types of Robinow syndrome, recessive form:

What causes Robinow syndrome, recessive form?

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

What are the symptoms of Robinow syndrome, recessive form?

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

Robinow syndrome, recessive form: Testing

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

Misdiagnosis: see misdiagnosis and Robinow syndrome, recessive form.

How is it treated?

Treatments for Robinow syndrome, recessive form: see treatments for Robinow syndrome, recessive form

Name of Robinow syndrome, recessive form

Main name of condition: Robinow syndrome, recessive form

 

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