HURLER SYNDROME - GENETIC DISEASES

Hurler syndrome



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Characteristics of Williams-Beuren Syndrome
Characteristics of Williams-Beuren Syndrome
Hurler syndrome is a rare genetic disease that manifests itself between 6 and 8 months of the baby and can lead to death by the age of 10. The disease is diagnosed when the first symptoms begin to appear, which involve difficulty breathing and fever. This syndrome causes the development of bone deformities, alteration of the cornea, heart problems, alteration of the bones of the face, short stature and intellectual impairment