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GTR Home > Conditions/Phenotypes > DPM3-congenital disorder of glycosylation

DPM3-congenital disorder of glycosylation

Synonyms
CDG Io; CDG1(DPM3); Congenital disorder of glycosylation type 1O; DPM3-CDG; MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15
Modes of inheritance
Autosomal recessive inheritance (Orphanet)

Summary

Limb-girdle muscular dystrophy-dystroglycanopathy type C15 (MDDGC15) is an autosomal recessive disorder characterized by progressive proximal muscle weakness, manifest initially as unsteady gait, but later including more distal muscles, and dilated cardiomyopathy. The age at onset varies widely from the first decade to adulthood; those with earlier onset may have delayed motor development. Laboratory studies show increased serum creatine kinase and muscle biopsy shows dystrophic features with decreased alpha-dystroglycan (DAG1; 128239). Biochemical studies often show evidence of abnormal N-glycosylation of serum proteins, consistent with a congenital disorder of glycosylation (CDG) (summary by Svahn et al., 2019). For a discussion of genetic heterogeneity of muscular dystrophy- dystroglycanopathy type C, see MDDGC1 (609308). For a discussion of the classification of CDGs, see CDG1A (212065). [from OMIM]

Available tests

37 tests are in the database for this condition.

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Clinical tests (37 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CDG1O, MDDGB15, MDDGC15, DPM3
    Summary: dolichyl-phosphate mannosyltransferase subunit 3, regulatory

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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