Diagnostic Difficulties of Mucopolysaccharidosis Type I Mild Forms: Clinical Cases
Mucopolysaccharidosis type I mild forms include Scheie syndrome and Hurler-Scheie syndrome that are characterized by slow progression, intact intelligence, and primarily effect on visual organ, musculoskeletal and cardiovascular systems. Early diagnostics, multidisciplinary approach to examination a...
Saved in:
| Main Authors: | Nato D. Vashakmadze, Leyla S. Namazova-Baranova, Natalia V. Zhurkova, Ekaterina Yu. Zakharova, Elena J. Voskobaeva, Marina A. Babaikina, Lyudmila M. Mikhaylova |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
"Paediatrician" Publishers LLC
2020-06-01
|
| Series: | Вопросы современной педиатрии |
| Subjects: | |
| Online Access: | https://vsp.spr-journal.ru/jour/article/view/2379 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Orthopedic Pathology in Children with Mucopolysaccharidosis Type I
by: Nato D. Vashakmadze, et al.
Published: (2016-12-01) -
Articular Syndrome Characteristics in Children with Mucopolysaccharidosis Type I
by: Nato D. Vashakmadze, et al.
Published: (2021-12-01) -
Mucopolysaccharidosis Type I (Hurler – Scheie Syndrome): Case Report
by: Nato D. Vashakmadze, et al.
Published: (2024-09-01) -
Differential Diagnosis of Hurler and Hurler–Scheie Syndromes: Clinical Case
by: Nataliya V. Buchinskaya, et al.
Published: (2025-05-01) -
Antibodies to recombinant human alpha-L-iduronidase prevent disease correction in cortical bone in MPS I mice
by: Sarah C. Hurt, et al.
Published: (2025-03-01)