Hypochondroplasia
Like other forms of dwarfism, it occurs when a fetus is still in the womb and there is a problem related to the cartilage converting into bone. It is considered a milder form of dwarfism.
Causes
Hypochondroplasia is the result of a genetic mutation.
Symptoms
Common signs and symptoms of hypochondroplasia are:
Disproportionately small hands, feet, arms and legs
Bowed legs that improve over time
Rounding of the back
Prominent forehead
Mild intellectual disability
Diagnosis
Because this is a milder form of dwarfism, the condition is often not apparent at birth. It can go undetected until early childhood or as late as adulthood.
To determine if your child has hypochondroplasia, your expert doctor will conduct a physical examination, review medical history and perform X-rays.