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GTR Home > Conditions/Phenotypes > Congenital disorder of deglycosylation

Summary

Excerpted from the GeneReview: NGLY1-Related Congenital Disorder of Deglycosylation
Individuals with NGLY1-related congenital disorder of deglycosylation (NGLY1-CDDG) typically display a clinical tetrad of developmental delay / intellectual disability in the mild to profound range, hypo- or alacrima, elevated liver transaminases that may spontaneously resolve in childhood, and a complex hyperkinetic movement disorder that can include choreiform, athetoid, dystonic, myoclonic, action tremor, and dysmetric movements. About half of affected individuals will develop clinical seizures. Other findings may include obstructive and/or central sleep apnea, oral motor defects that affect feeding ability, auditory neuropathy, constipation, scoliosis, and peripheral neuropathy.

Available tests

27 tests are in the database for this condition.

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Genes See tests for all associated and related genes

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