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...

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Bibliographic Details
Main Authors: Dan Cristian Gheorghe, Adina Zamfir-Chiru-Anton, AE Stanciu
Format: Article
Language:English
Published: Amaltea Medical Publishing House 2020-03-01
Series:Romanian Medical Journal
Subjects:
Online Access:https://rmj.com.ro/articles/2020.1/RMJ_2020_1_Art-16.pdf