Aspartylglucosaminuria (Q61129): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed label, description and/or aliases in pt-br, en
description / pt-brdescription / pt-br
 
A aspartilglicosaminúria é uma doença autossômica recessiva de depósito lisossomal pertencente ao grupo da oligossacaridose, devido à deficiência de N-aspartilglicosaminidase. Os sinais clínicos incluem deficiência intelectual de desenvolvimento lento, começando com falta de jeito, fala tardia e hipercinesia, dismorfismo facial leve e cifoescoliose leve.
description / endescription / en
 
Aspartylglycosaminuria is an autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group that is due to deficiency in N-aspartylglycosaminidase. Clinical signs include slowly developing intellectual deficit, beginning with clumsiness, late speech, and hyperkinesia, mild facial dysmorphism, and slight kyphoscoliosis.

Revision as of 08:37, 14 August 2026

Aspartylglycosaminuria is an autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group that is due to deficiency in N-aspartylglycosaminidase. Clinical signs include slowly developing intellectual deficit, beginning with clumsiness, late speech, and hyperkinesia, mild facial dysmorphism, and slight kyphoscoliosis.
Language Label Description Also known as
default for all languages
ID_2143470200
    English
    Aspartylglucosaminuria
    Aspartylglycosaminuria is an autosomal recessive lysosomal storage disease belonging to the oligosaccharidosis group that is due to deficiency in N-aspartylglycosaminidase. Clinical signs include slowly developing intellectual deficit, beginning with clumsiness, late speech, and hyperkinesia, mild facial dysmorphism, and slight kyphoscoliosis.

      Statements