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Achondrogenesis type 1B

Achondrogenesis type 1B: Introduction

Achondrogenesis type 1B: A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine. More detailed information about the symptoms, causes, and treatments of Achondrogenesis type 1B is available below.

Symptoms of Achondrogenesis type 1B

Wrongly Diagnosed with Achondrogenesis type 1B?

Achondrogenesis type 1B: Deaths

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Achondrogenesis type 1B: Complications

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Causes of Achondrogenesis type 1B

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Disease Topics Related To Achondrogenesis type 1B

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Achondrogenesis type 1B: Research Doctors & Specialists

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Evidence Based Medicine Research for Achondrogenesis type 1B

Medical research articles related to Achondrogenesis type 1B include:

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Achondrogenesis type 1B: Animations

Research about Achondrogenesis type 1B

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Statistics for Achondrogenesis type 1B

Achondrogenesis type 1B: Broader Related Topics

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Definitions of Achondrogenesis type 1B:

Achondrogenesis type 1B is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Achondrogenesis type 1B, or a subtype of Achondrogenesis type 1B, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Achondrogenesis type 1B Info

More information about Achondrogenesis type 1B

  1. Achondrogenesis type 1B: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
  7. Complications
 

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