5C56.31Ангилал
Mucopolysaccharidosis type 2
Тодорхойлолт
Mucopolysaccharidosis type 2 (MPS 2) is a lysosomal storage disease belonging to the group of mucopolysaccharidoses. The clinical picture ranges from severe (the most frequent form) with early psychomotor regression, facial dysmorphism (macroglossia, constantly opened mouth, coarse features), hepatosplenomegaly, limited joint motion, carpal tunnel syndrome, dysostosis multiplex, small size, behavioural disorders and psychomotor regression leading to intellectual deficit, deafness, cardiac and respiratory disorders, and cutaneous signs, to mild (normal intelligence, milder dysmorphism and dysostoses).
Оруулагдах онош Inclusions
- Hunter syndrome
Индексийн нэр томьёо Index terms · 20
Mucopolysaccharidosis type 2Iduronate 2-sulfatase deficiencyHunter syndromeiduronate 2-sulphatase deficiencyiduronate sulfatase deficiencyiduronate sulphatase deficiencysulfo-iduronate sulfatase deficiencysulfoiduronidate sulfatase deficiencysulpho-iduronate sulphatase deficiencysulphoiduronidate sulphatase deficiencyMPS2 - [mucopolysaccharidosis 2]Mucopolysaccharidosis type 2AIduronate 2-sulfatase deficiency type AHunter syndrome type AMucopolysaccharidosis type 2, severe formMucopolysaccharidosis type 2BIduronate 2-sulfatase deficiency type BHunter syndrome type BMucopolysaccharidosis type 2, mild formMucopolysaccharidosis type 2, attenuated form
Монгол орчуулга хянагдаж байгаа тул англи эхийг харуулж байна. Эх сурвалж: WHO ICD-11 (MMS) · WHO сайтад харах ↗