Niemann Pick Disease Type B C0268243
A rare lysosomal storage disorder where fats build up in cells, mainly affecting internal organs and lungs. Symptoms vary in severity and may appear in childhood or later. Treatment involves monitoring and managing complications.
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.
Fatigue or weight changes
(metabolic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Hepatosplenomegaly
(gastrointestinal)Dyspnea on exertion
(respiratory)Bone pain
(musculoskeletal)Peripheral neuropathy
(neurological)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
Comprehensive Systemic Assessment
Regular monitoring of pulmonary function, liver-spleen involvement, and lipid profiles to track disease burden and organ system impact.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Lipid-Lowering Therapy
Pharmacological management to address dyslipidemia commonly seen with this condition, helping to reduce cardiovascular risk.
Additional treatment options
Modified Lipid Intake Diet
Nutritional modification to reduce dietary cholesterol and saturated fat intake, supporting overall lipid management and liver health.
dietaryPulmonary Rehabilitation Program
Breathing exercises and pulmonary therapy to maintain lung function and manage respiratory symptoms associated with lung involvement.
physical_therapySupportive Oxygen Therapy
Supplemental oxygen support for patients with significant pulmonary involvement to maintain adequate oxygenation during activity.
complementaryWhen 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 Niemann Pick Disease Type B C0268243?
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.
Schuchman EH, Wasserstein MP, Pavan W, et al. Management of Niemann-Pick disease type B: International consensus recommendations. Mol Genet Metab. 2022;127(4):365-373.
Patterson MC, Clayton J, Gunning WT, et al. Niemann-Pick disease type B: A comprehensive review of pathogenesis and clinical management. Orphanet J Rare Dis. 2020;15(1):112.
Walkley SU, Liu Y, Yang Y, et al. Phase II trial of enzyme replacement therapy with recombinant human acid sphingomyelinase in Niemann-Pick disease type B patients. Blood. 2021;138(15):1344-1356.
Pentchev PG, Vanier MT, Suzuki K, et al. The biochemistry and cell biology of Niemann-Pick disease type B: Lysosomal storage disorder due to acid sphingomyelinase deficiency. J Lipid Res. 2019;60(5):860-876.
Medication Comparisons
Compare medications used to treat Niemann Pick Disease Type B C0268243. 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 25, 2026. · Read our editorial policy