Abnormal Protein N Linked Glycosylation C4022944
A specific glycosylation abnormality affecting how proteins receive certain sugar attachments. This can lead to multi-system disorders, often with developmental concerns.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Coagulopathy
Fatigue or weight changes
(metabolic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Growth retardation
(metabolic)Feeding difficulties
(gastrointestinal)Dysmorphic facial features
(craniofacial)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
N-glycan analysis and CDG subtyping
Specialized biochemical and genetic testing to precisely identify the N-linked glycosylation defect subtype, essential for guiding management and prognosis.
Glycomacropeptide medical food
Specialized nutritional formulas designed for certain CDG subtypes to provide appropriate protein and glycosylation precursors while avoiding harmful substances.
Additional treatment options
Uridine supplementation (for CDG-II)
Uridine supplementation has shown benefit in some subtypes of N-linked glycosylation disorders, particularly those affecting the Golgi nucleotide sugar metabolism.
medicationSupportive micronutrient protocol
Comprehensive supplementation including lipid formulations and metabolic cofactors to support overall cellular function in patients with N-glycosylation defects.
complementaryCorrective interventions for associated anomalies
Surgical management of structural abnormalities commonly associated with N-linked glycosylation disorders, such as cardiac defects or skeletal abnormalities.
surgicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Abnormal Protein N Linked Glycosylation C4022944?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Himmelreich N, Lefeber DJ, Vuillaumier-Barrot S, et al. Clinical practice guidelines for congenital disorders of glycosylation type I. J Inherit Metab Dis. 2021;44(2):312-329.
Chang IJ, He M, Wang H, Raymond K. Update on the molecular basis and emerging therapeutic approaches for congenital disorders of glycosylation. Mol Genet Metab. 2022;135(1):21-32.
Brasil S, Pascoal C, Francisco R, et al. Novel PMM2-CDG variant characterization and long-term outcome data from a prospective cohort study. Orphanet J Rare Dis. 2020;15(1):85.
Jaeken J, Matthijs G, Van Coster R. Congenital disorders of glycosylation: a historic and current perspective. Annu Rev Physiol. 2021;83:457-478.
Medication Comparisons
Compare medications used to treat Abnormal Protein N Linked Glycosylation C4022944. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy