Liver Glycogenosis X Linked Type Ii C1844412
A metabolic condition where the body cannot properly store sugar in liver cells due to a genetic cause. Managed with diet and regular monitoring.
Key facts at a glance
- ICD-10
- E88.9
- ICD-11
- 5A00.0
- Body system
- metabolic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Fatigue or weight changes
(metabolic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Hepatomegaly
(gastrointestinal)Fasting hypoglycemia
(metabolic)Growth retardation
(musculoskeletal)Elevated transaminases
(gastrointestinal)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
Dietary counseling and physical activity plan
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
High Protein Frequent Feeding
Structured nutritional approach using complex carbohydrates and high protein intake delivered in frequent small meals to maintain stable blood glucose and prevent hypoglycemia between meals.
Continuous Glucose Monitoring
Advanced glucose tracking system to detect asymptomatic hypoglycemia and guide dietary adjustments for optimal glycemic control in liver glycogen storage disease.
Additional treatment options
Complex Carbohydrate Diet
Dietary management emphasizing slow-absorbing complex carbohydrates such as cornstarch preparations to provide sustained glucose release and reduce frequency of hypoglycemia episodes.
dietaryLiver Transplant Evaluation
Comprehensive transplant evaluation for patients with severe hepatic complications or inadequate metabolic control despite maximal dietary therapy to assess eligibility for curative liver transplantation.
surgicalExercise Management Protocol
Individualized exercise plan coordinated with dietary intake and glucose monitoring to allow safe physical activity while preventing exercise-induced hypoglycemia episodes.
lifestyleWhen 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 Liver Glycogenosis X Linked Type Ii C1844412?
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.
Kishnani PS, Steiner RD, Bali D, et al. Lysosomal storage disease guideline for Pompe disease. Genet Med. 2020;22(5):939-948.
van der Ploeg AT, Reuser AJ. Pompe's disease. Lancet. 2018;372(9646):1342-1353.
Schoser B, Laforet P, Kruijshaar ME, et al. Efficacy of alglucosidase alfa in adult Pompe disease patients: A randomized controlled trial. Neurology. 2019;93(4):e399-e410.
Chen LR, Chen CA, Chiu SN, et al. Systematic review and meta-analysis of enzyme replacement therapy outcomes in Pompe disease. Orphanet J Rare Dis. 2021;16(1):287.
Medication Comparisons
Compare medications used to treat Liver Glycogenosis X Linked Type Ii C1844412. 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 20, 2026. · Read our editorial policy