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Chromosome 1, monosomy 1q25 q32

Chromosome 1, monosomy 1q25 q32: Introduction

Chromosome 1, monosomy 1q25 q32: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as digital defects, facial dysmorphism, retarded growth, mental retardation and spasticity. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1q25 q32 is available below.

Symptoms of Chromosome 1, monosomy 1q25 q32

Causes of Chromosome 1, monosomy 1q25 q32

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Chromosome 1, monosomy 1q25 q32: Broader Related Topics

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Definitions of Chromosome 1, monosomy 1q25 q32:

Chromosome 1, monosomy 1q25 q32 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 1, monosomy 1q25 q32, or a subtype of Chromosome 1, monosomy 1q25 q32, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 1, monosomy 1q25 q32

  1. Chromosome 1, monosomy 1q25 q32: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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