Liberal Dictionary English Dictionary

gangliosidosis

n.

Any of a group of diseases marked by abnormal accumulation of gangliosides within the nervous system.

Individuals with GM1 gangliosidosis type I usually do not survive past early childhood. — GM1 gangliosidosis – Genetics Home Reference – NIH

GM1 Gangliosidosis — GM1 Gangliosidosis: Find Best Doctors and Hospitals | Xpertdox

Download figure — Peripheral blood findings in GM1 gangliosidosis | Blood Journal

GM1 gangliosidosis type II. Facial appearance at autopsy. Mild anomalies of the ear and — Lysosomal storage diseases – IOS Press

Type 3 GM1 gangliosidosis is characterized by onset around the second decade of life with slowly progressive extrapiramidal signs, such as dystonia and — Facial grimacing as a clue for the diagnosis of GM1 type 3

Download figure — MR Imaging Findings in 2 Cases of Late Infantile GM1 Gangliosidosis

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