Published January 1, 2020
| Version v1
Journal article
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Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG
Creators
- 1. Dokuz Eylul Univ, Sch Med, Dept Paediat Neurol, Izmir, Turkey
- 2. Barcelona Inst Sci & Technol, Ctr Genom Regulat, CNAG CRG, Barcelona, Spain
- 3. Univ Cambridge, Dept Clin Neurosci, Cambridge, England
Description
Background: Congenital disorders of glycosylation (CDG) is a heterogeneous group of congenital metabolic diseases with multisystem clinical involvement. ALG3-CDG is a very rare subtype with only 24 cases reported so far.
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