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Chromosome 10p terminal deletion syndrome

Chromosome 10p terminal deletion syndrome: Introduction

Chromosome 10p terminal deletion syndrome: A very rare syndrome caused by a chromosomal defect (10p terminal deletion) and can result in a variety of malformations that are similar to DiGeorge syndrome and velocardiofacial syndrome. More detailed information about the symptoms, causes, and treatments of Chromosome 10p terminal deletion syndrome is available below.

Symptoms of Chromosome 10p terminal deletion syndrome

Causes of Chromosome 10p terminal deletion syndrome

Read more about causes of Chromosome 10p terminal deletion syndrome.

Statistics for Chromosome 10p terminal deletion syndrome

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Definitions of Chromosome 10p terminal deletion syndrome:

Chromosome 10p terminal deletion syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 10p terminal deletion syndrome, or a subtype of Chromosome 10p terminal deletion syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 10p terminal deletion syndrome

  1. Chromosome 10p terminal deletion syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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