[The role of ophthalmological examination in the diagnosis of gangliosidosis GM1]. / Znaczenie badania okulistycznego w rozpoznawaniu gangliozydozy GM1.
Klin Oczna
; 113(7-9): 266-9, 2011.
Article
em Pl
| MEDLINE
| ID: mdl-22256571
ABSTRACT
Gangliosidosis GM1 belongs to a group of lysosomal storage diseases and results from the deficiency of acidic beta-galactosidase activity. The enzyme is essential for the degradation of ganglioside GM1 and its derivatives. The disease causes multi-organ injury, however accumulation of ganglioside GM1 mainly in the brain white and gray matter results in predomination of neurological symptoms. Based on the actual knowledge--the condition is untreatable and especially in the very severe infantile form, the duration of the survival is very short. One of the characteristic symptoms of some lysosomal storage diseases, including gangliosidosis GM1, is "cherry-red" spot found in the fundus of the eye. In the publication the clinical course of gangliosidosis GM1 in two infants is presented. The value of an ophthalmological examination in the diagnosis of this rare condition has been emphasized.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Doenças Retinianas
/
Gangliosidose GM1
/
Técnicas de Diagnóstico Oftalmológico
/
Fundo de Olho
Tipo de estudo:
Diagnostic_studies
Limite:
Humans
/
Infant
/
Male
/
Newborn
Idioma:
Pl
Revista:
Klin Oczna
Ano de publicação:
2011
Tipo de documento:
Article