Pediatric Achondroplasia (Dwarfism)
Achondroplasia (dwarfism) is a rare genetic disorder causing cartilage to not form normally.
What is Pediatric Achondroplasia (Dwarfism)?
Achondroplasia is an autosomal dominate disease which means that only one abnormal gene inherited from a single parent can lead to this condition. Boys reach an average height of about 4 feet, 4 inches. Girls reach an average height of about 4 feet, 1 inch.
Risk factors
Most babies born with achondroplasia have no family history of it. However, having a parent with achondroplasia increases the risk of being born with this condition.
What are the signs and symptoms of Pediatric Achondroplasia (Dwarfism)?
Bowed lower legs
Flat feet
Large head/forehead
Poor muscle tone and loose joints
Short arms, legs and fingers with normal-sized torso
How is Pediatric Achondroplasia (Dwarfism) diagnosed?
DNA testing
Fetal ultrasound
Pediatric Achondroplasia (Dwarfism) Doctors and Providers
![doctor](https://www.childrens.com/wps/wcm/connect/childrenspublic/a3047508-fac6-4f64-8b75-97c5869392c3/Bruno-Braga.gif?MOD=AJPERES&CACHEID=ROOTWORKSPACE.Z18_6IH81240MO2M00A9420PHQ3004-a3047508-fac6-4f64-8b75-97c5869392c3-oJOwczJ)
Bruno Braga, MDPediatric Neurosurgeon
![doctor](https://www.childrens.com/wps/wcm/connect/childrenspublic/1eb11513-80e6-4fb2-b775-3950bcd7a134/Dale-Swift.jpeg?MOD=AJPERES&CACHEID=ROOTWORKSPACE.Z18_6IH81240MO2M00A9420PHQ3004-1eb11513-80e6-4fb2-b775-3950bcd7a134-oD-bu3r)
Dale Swift, MDPediatric Neurosurgeon