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“Inborn Genetic Dwarfism Issues”  

  In our body's bones, Inborn Genetic Dwarfism Issues are inborn genetic conditions, including many developmental bone dis-orders (bone dysplasias), experienced as part of dwarfism characterized by short stature, abnormal skeletal growth and undersize.
  Examples of conditions that include inborn genetic dwarfism issues:

• Cockayne's syndrome

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“Dwarfisms (Nanosomia)”  

Dwarfism

  In our body, Dwarfism is a hereditary trait (genetic) or pathological anomaly, involving many inborn genetic dwarfism issues, characterized by short stature, abnormal skeletal growth and undersize.
  In our adult body, Dwarfism is a dis-order, indicative to a specific set of signs, symptoms or other health indicators, associated with an undersized body health challenges.

In our body, most Dwarfisms are caused by inherited or spontaneous mutations in the FGFR3 genes, or with deletions of the X chromosome.
  Examples of groupings for dwarfisms may include:

• primordial dwarfism
• rhizomelic dwarfism

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