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Chromosome 1, monosomy 1q4

Chromosome 1, monosomy 1q4: Introduction

Chromosome 1, monosomy 1q4: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as facial dysmorphism, retarded fetal growth, seizures, mental retardation, testicular problems and kidney defects. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1q4 is available below.

Symptoms of Chromosome 1, monosomy 1q4

Causes of Chromosome 1, monosomy 1q4

Read more about causes of Chromosome 1, monosomy 1q4.

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Definitions of Chromosome 1, monosomy 1q4:

Chromosome 1, monosomy 1q4 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 1q4, or a subtype of Chromosome 1, monosomy 1q4, 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 1q4

  1. Chromosome 1, monosomy 1q4: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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