Intracerebroventricular Enzyme Replacement Therapy in Patients with Neuropathic Form of Mucopolysaccharidosis Type II: to Help Practicing Physician

Mucopolysaccharidosis type II (Hunter syndrome, MPS II) is a rare hereditary disease from the group of hereditary metabolic diseases. There are neuropathic and non-neuropathic forms of this disease. The neuropathic form is most common and leads to severe cognitive impairment and progressive damage o...

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Главные авторы:	Nataliya V. Zhurkova, Nato D. Vashakmadze, Georgiy A. Karkashadze, Elena V. Kaytukova
Формат:	Artigo
Язык:	Inglês
Опубликовано:	"Paediatrician" Publishers LLC 2024-09-01
Серии:	Вопросы современной педиатрии
Предметы:	mucopolysaccharidosis type ii hunter syndrome neuropathic form of mps ii intracerebroventricular enzyme replacement therapy
Online-ссылка:	https://vsp.spr-journal.ru/jour/article/view/3572
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