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NGLY1 Deficiency: A Rare Newly Described Condition with a Typical Presentation
Ivana Dabaj1, Bénédicte Sudrié-Arnaud2, François Lecoquierre3
1Department of Neonatal Pediatrics, Intensive Care and Neuropediatrics, Normandie University, UNIROUEN, CHU Rouen, INSERM U1245, 76000 Rouen, France.
NGLY1 deficiency, a rare genetic disorder, was identified in a French patient with developmental delay and other symptoms. Diagnosis involved genetic sequencing and urine analysis, confirming the condition and its associated features.
Area of Science:
- Biochemistry
- Genetics
- Rare Diseases
Background:
- N-linked deglycosylation (NGLY1-CDDG) is an autosomal recessive disorder.
- NGLY1 deficiency is a severe, multisystemic disease often diagnosed via exome or genome sequencing.
- Limited knowledge exists regarding NGLY1 deficiency, necessitating detailed case reports.
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