𝔖 Bobbio Scriptorium
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Mongolian spots and GM1 type 1 gangliosidosis

✍ Scribed by Burton Esterly, Nancy; Weissbluth, Marc; Caro, William A.


Book ID
120883311
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
182 KB
Volume
22
Category
Article
ISSN
1097-6787

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## Abstract GM1 gangliosidosis is due to β‐galactosidase deficiency. Only patients with type 3 disease survive into adulthood and develop movement disorders. Clinical descriptions of this form are rare, particularly in non‐Japanese patients. We describe four new patients and systematically analyze