Browsing by Subject "MUTACION"
Now showing items 1-2 of 2
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First clinical and genetic description of a family diagnosed with late-onset Pompe disease from Costa Rica
(2017)Glycogen storage disease type II, also known as Pompe disease, is an autosomal recessive disorder caused by deficiency of enzymatic activity of acid alpha-glucosidase. The wide phenotypical variation of this disease relates ... -
Mucopolisacaridosis II: nueva mutación patogénica en gen IDS
(Colegio de Médicos y Cirujanos de Costa Rica, 2014-12)La mucopolisacaridosis tipo II es una enfermedad lisosomal producida por la deficiencia de la enzima iduronato 2 sulfatasa. Es una condición infrecuente de herencia recesiva ligada al X, que puede producir importante ...