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Chromosome 3, Monosomy 3p2

Chromosome 3, Monosomy 3p2: Introduction

Chromosome 3, Monosomy 3p2: A very rare chromosomal disorder involving the deletion of the end portion of short arm of chromosome 3. Symptoms vary according to the exact size and location of the deletion. More detailed information about the symptoms, causes, and treatments of Chromosome 3, Monosomy 3p2 is available below.

Symptoms of Chromosome 3, Monosomy 3p2

Causes of Chromosome 3, Monosomy 3p2

Read more about causes of Chromosome 3, Monosomy 3p2.

Disease Topics Related To Chromosome 3, Monosomy 3p2

Research the causes of these diseases that are similar to, or related to, Chromosome 3, Monosomy 3p2:

  • Prenatal and postnatal growth deficiency; severe to profound mental retardation; distinctive malformations of the skull and facial (craniofacial) region; eyebrows that grow together (synophrys)
  • Excessive hair growth (hypertrichosis)
  • more related diseases...»

Less Common Symptoms of Chromosome 3, Monosomy 3p2

Statistics for Chromosome 3, Monosomy 3p2

Chromosome 3, Monosomy 3p2: Broader Related Topics

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Definitions of Chromosome 3, Monosomy 3p2:

Chromosome 3, Monosomy 3p2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 3, Monosomy 3p2, or a subtype of Chromosome 3, Monosomy 3p2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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Videos about Chromosome 3, Monosomy 3p2

 

More information about Chromosome 3, Monosomy 3p2

  1. Chromosome 3, Monosomy 3p2: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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