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Spondylocarpotarsal synostosis

Spondylocarpotarsal synostosis: Introduction

Spondylocarpotarsal synostosis: A rare genetic disorder characterized by short stature, fusion of toe and finger bones and failure of spinal segmentation. More detailed information about the symptoms, causes, and treatments of Spondylocarpotarsal synostosis is available below.

Symptoms of Spondylocarpotarsal synostosis

Wrongly Diagnosed with Spondylocarpotarsal synostosis?

Spondylocarpotarsal synostosis: Related Patient Stories

Spondylocarpotarsal synostosis: Complications

Review possible medical complications related to Spondylocarpotarsal synostosis:

Causes of Spondylocarpotarsal synostosis

Read more about causes of Spondylocarpotarsal synostosis.

Disease Topics Related To Spondylocarpotarsal synostosis

Research the causes of these diseases that are similar to, or related to, Spondylocarpotarsal synostosis:

Less Common Symptoms of Spondylocarpotarsal synostosis

Misdiagnosis and Spondylocarpotarsal synostosis

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Spondylocarpotarsal synostosis: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Spondylocarpotarsal synostosis: Animations

Statistics for Spondylocarpotarsal synostosis

Spondylocarpotarsal synostosis: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Spondylocarpotarsal synostosis, or answer someone else's question, on our message boards:

Definitions of Spondylocarpotarsal synostosis:

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


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