NGLY1 deficiency

NGLY1 deficiency or NGLY1-congenital disorder of deglycosylation is a very rare genetic disorder caused by mutations in NGLY1. It is an autosomal recessive disorder. Errors in deglycosylation are responsible for the symptoms of this condition.^[1] Clinically, most affected individuals display developmental delay, lack of tears, elevated liver transaminases and a movement disorder.^[2] NGLY1 deficiency is difficult to diagnose, and most individuals have been identified by exome sequencing.

NGLY1 deficiency causes a dysfunction in the endoplasmic reticulum-associated degradation pathway. NGLY1 encodes an enzyme, N-glycanase 1, that cleaves N-glycans. Without N-glycanase, N-glycosylated proteins that are misfolded in the endoplasmic reticulum cannot be degraded, and thus accumulate in the cytoplasm of cells.^[3][4]

Signs and symptoms

Clinical findings in NGLY1 deficiency are not specific, however four common findings have been identified in a majority of patients. These four findings include developmental delay or intellectual disability of varying degrees, lack or or greatly reduced tears, elevated liver transaminases, and a complex movement disorder. The elevated liver enzymes often resolve in childhood. In addition, approximately 50% of patients described with NGLY1 deficiency have seizures, which can vary in their difficulty to control. Other findings that have been reported in affected individuals include sleep apnea, constipation, scoliosis, oral motor defects, auditory neuropathy and peripheral neuropathy.^[2]

Diagnosis

NGLY1 deficiency can be suspected based on clinical findings, however confirmation of the diagnosis requires the identification of biallelic pathogenic variants in NGLY1. Traditional screening tests utilized for congenital disorders of glycosylation, including carbohydrate deficient transferrin are not diagnostic in NGLY1 deficiency. To date all variants identified as being causative of NGLY1 deficiency have been sequence variants, rather than copy number variants. This spectrum may change as additional cases are identified.^[2] A common nonsense variant (c.1201A>T (p.Arg401Ter)) accounts for approximately 1/3 of pathogenic variants identified, and is associated with a more severe clinical course.^[2]

Treatment

There is no cure for NGLY1 deficiency.^[5] Supportive care is indicated for each patient based on their specific symptoms, and can include eye drops to manage the alacrima, pharmaceutical management of seizures, feeding therapy and physical therapy.^[2] Most potential treatment options for NGLY1 deficiency are in the pre-clinical stages. These include enzyme replacement therapy, as well as ENGase inhibitors.^[2]

Epidemiology

Eighteen patients with confirmed NGLY1 deficiency have been reported in the medical literature.^[2] Patient databases managed through disease specific support groups have reported 46 patients.^[2][6] Currently, the majority of individuals reported with NGLY1 deficiency are of northern European descent, however this likely reflects an ascertainment bias in these early stages of the disorder. Affected individuals with African and Hispanic backgrounds have been identified.^[2].

History

The first cases of NGLY1 deficiency were described in 2012.^[1] NGLY1 deficiency has received a large amount of attention, despite its rarity, due to the children of two media-savvy families being afflicted.^[7] The Wilseys, descendants of Dede Wilsey, founded the Grace Science Foundation in honor of their daughter, and Matt Might and his wife founded the Bertrand Might Research Fund. These foundations have contributed millions of dollars to research efforts.^[7][8]

See also

• Glycobiology

References

External links