Complete Information on Ectodermal Dysplasia

The dysplasia of Ectodermal it is one be hereditary characterized through abnormal development of the skin, hats, the nail, the teeth and the glands of the sweat. There are many different types of ectodermal dysplasia. Many dysplasies ectodermal of cause of gene defects. The most common form of dysplasy ectodermal is related to the chromosome of X and assigns usually men. Other forms of the disease assign men and women also. Dysplasies of Ectodermal are caused by changed genes. The changed genes can be inherited or the normal genes can become defective (undergo a change) per hour of the design. A common type of ED affects males more than females.

 The antenatal diagnosis is available for some families with the X-dependent dysplasy ectodermal hypohidrotic, by the use of the probes of DNA. The prevalence of the various types of ED is thought to be approximately 7 in 10.000 births of phase. The dysplasies of Ectodermal can occur in any race but are much more dominant in the Caucasians than any other group and particularly in the right Caucasians. The people with the dysplasy ectodermal can sweat or not have decreased perspiration because of a lack of glands of sweat.

The children with this disease have fevers of management of difficulty. The soft disease can produce strongly high fevers, because the can't of skin sweated and orders the temperature correctly. The affected adults cannot tolerate a hot environment and to need special measures to keep a normal temperature of body. There is no specific treatment for this disorder. A child with the dysplasy ectodermal can meet social and emotive challenges single in this condition. The organizations and the resources of support are available for children and their families. The port of a wig and dentures can improve the aspect of the child. The synthetic tears can be necessary to replace the normal tearing and to prevent to dry of the eyes.