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Chromosome 1, monosomy 1q32 q42

Chromosome 1, monosomy 1q32 q42: Introduction

Chromosome 1, monosomy 1q32 q42: A rare chromosomal disorder where deletion of a portion of chromosome 1 causes various abnormalities such as fetal or newborn death, facial dysmorphism, short stature, finger defects and various other anomalies. More detailed information about the symptoms, causes, and treatments of Chromosome 1, monosomy 1q32 q42 is available below.

Symptoms of Chromosome 1, monosomy 1q32 q42

Causes of Chromosome 1, monosomy 1q32 q42

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Definitions of Chromosome 1, monosomy 1q32 q42:

Chromosome 1, monosomy 1q32 q42 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 1q32 q42, or a subtype of Chromosome 1, monosomy 1q32 q42, 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 1q32 q42

  1. Chromosome 1, monosomy 1q32 q42: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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