ACHONDROPLASIA is known as being undersized, or less than 50in. in height. Having short limbs, a normal sized trunk, large head with a depressed nasal bridge and small face. This is a result of a disease in the thyroid gland. It can also be caused by Down syndrome or absorption, a cartilaginous tissue during the fetal stage. Hypochondroplasia, a mild form of dwarfism. Spinal tuberculosis and the deficiency of the pituitary gland secretions. Treatment with …showed first 75 words of 497 total…

…showed last 75 words of 497 total…autosomal dominant condition. This means a person with achondroplasia has a 50% chance of passing it to his children. 75% of individuals with achondroplasia are born to normal size parents. The gene for Dwarfism, fibroblast growth factor receptor 3 (FGFR3) is acquired when one undersized individual and a normal sized individual produce a child. Couples at risk of having a child with 2 copies of the changed gene. A DNA test is now also available to detect double homozygosity.