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Галактосіалідоз

ORPHA:351· ICD-10 E77.1· Galactosialidosis

Визначення(English summary)

Galactosialidosis is a lysosomal storage disease characterized by coarse facial features, macular ''cherry red spot'', and dysostosis multiplex. Clinical presentation can be heterogenous ranging from a severe, early-onset, rapidly progressive infantile form to late onset, slowly progressive juvenile/adult form.

Поширеність
Unknown
Успадкування
Autosomal recessive
Вік початку
All ages