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Robinow syndrome, autosomal recessive

Robinow syndrome, autosomal recessive: Introduction

Robinow syndrome, autosomal recessive: A rare genetic disorder characterized by a flat face, short forearms, vertebral anomalies and hypoplastic genitalia. More detailed information about the symptoms, causes, and treatments of Robinow syndrome, autosomal recessive is available below.

Symptoms of Robinow syndrome, autosomal recessive

Home Diagnostic Testing

Home medical testing related to Robinow syndrome, autosomal recessive:

Wrongly Diagnosed with Robinow syndrome, autosomal recessive?

Robinow syndrome, autosomal recessive: Complications

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Causes of Robinow syndrome, autosomal recessive

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Disease Topics Related To Robinow syndrome, autosomal recessive

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

Less Common Symptoms of Robinow syndrome, autosomal recessive

Robinow syndrome, autosomal recessive: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Robinow syndrome, autosomal recessive

Mild worm infections undiagnosed in children: Human worm infestations, esp. threadworm, can be overlooked in some cases, because it may cause only mild or even absent symptoms. Although the most...read more »

Mesenteric adenitis misdiagnosed as appendicitis in children: Because appendicitis is one of the more feared conditions for a child with abdominal pain, it can be over-diagnosed (it can, of course, also fail to be...read more »

Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue with hyperension, arises in relation to the simple equipment used...read more »

Children with migraine often misdiagnosed: A migraine often fails to be correctly diagnosed in pediatric patients. These patients are not the typical migraine sufferers, but migraines can also occur in children....read more »

Robinow syndrome, autosomal recessive: Research Doctors & Specialists

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Hospitals & Clinics: Robinow syndrome, autosomal recessive

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Statistics for Robinow syndrome, autosomal recessive

Robinow syndrome, autosomal recessive: Broader Related Topics

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Definitions of Robinow syndrome, autosomal recessive:

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

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More information about Robinow syndrome, autosomal recessive

  1. Robinow syndrome, autosomal recessive: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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