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It is one of the oldest known birth defects. Achondroplasia a nonlethal sort of chondrodysplasia or osteochondrodysplasias and is featured by abnormal bone growth that consequences in short stature with disproportionately short legs, short arms, a large head, characteristic features of face with frontal bossing, a normal trunk length, genu verum, prominent lumbar lordosis which is also known as kyphosis, a trident hand configuration, and mid-face hypoplasia. It is basically inherited as a mandolin autosomal dominant trait which means that child will have the disorder if a child gets the defected gene from parents. The chance of getting the disorder increases to 50% if the one of parents have Achondroplasia which increases to above than 70% if both of the parents have same problem. But in some cases it happens that parent may give birth to a child who has Achondroplasia when none of the parents have that problem. Hypotonic is very common and typical in infants and acquisition of production motor milestone is delayed many times. Approximately 80% of its cases are because of new or de novo dominant mutation and its mutation rate are estimated to be 0.000014 per gamete per generation. It can be said by a rough approximation that every one out of 25 thousand births face this problem. Although there is no specific treatment for this disease yet it can be diagnosed before birth with help of prenatal ultrasound which may show excessive amniotic fluid around the unborn baby. Symptoms of this are typical which are also visible at birth like bowed legs, abnormal appearance of hand with persistent space between the ring and the long fingers, very prominent forehead, spinal stenosis, spine curvature which is called lordosis or kyphosis. But intelligence is generally very normal with Achondroplasia patients with brain enlargement very common.