Apert Syndrome

Apert Syndrome Apert Syndrome (AKA Alport syndrome) is a genetic defect which can be acquire from a p arnt who has Apert or a fresh mutation. It pop off under the broad classification of craniofacial/limb anomalies. Approximately 1 per 160,000 to 200,000 live births inherit it. Some symptoms that Apert sufferers have argon opposed heart defects, ear infections, severe acne, increased incidence of summarize injuries, and many more. The skull is prematurely fused and unable to grow normally, and the fingers and toes are fused together in varying degrees.

If your barbarian gets Apert Synd rome they whitethorn have many physical defects as well as a few other problems such as poky learning, a cleft palate, vision problems, and problems with acne during puberty. I dont think Apert Syndrome fryren die, expecially because you can pass Apert through genetics. A child with Apert Syndrome could live a pretty normal life. The mutation which causes Apert Syndrome is ingraft on chrom...If you want to get a full essay, limit it on our website: BestEssayCheap.com

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