DPM3 congenital disorder of glycosylation (Q94040): Difference between revisions
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O distúrbio congênito de glicosilação tipo 1O (CDG-Io) é uma forma extremamente rara de síndrome CDG caracterizada clinicamente no único caso relatado por fraqueza muscular, marcha gingada e cardiomiopatia dilatada. | |||
| description / en | description / en | ||
Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy. | |||
Revision as of 09:09, 16 August 2026
Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1389256016 |
||
| English | DPM3 congenital disorder of glycosylation |
Congenital disorder of glycosylation type 1o (CDG-Io) is an extremely rare form of CDG syndrome characterised clinically in the single reported case by muscle weakness, waddling gait, and dilated cardiomyopathy. |
