Hunter syndrome revisited
Hunter syndrome is the type II of mucopolysaccharidose. With impaired glycosaminoglycan catabolism, heparan and dermatan sulfate accumulate in lysosomes. Multiple organ dysfunction is a consequence of this effect. We present the case of a a 9 year-old boy was refered to our department for breathing...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Amaltea Medical Publishing House
2020-03-01
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Series: | Romanian Medical Journal |
Subjects: | |
Online Access: | https://rmj.com.ro/articles/2020.1/RMJ_2020_1_Art-16.pdf |