Uniparental Disomy Of 7 C2931632
A rare genetic condition where both copies of chromosome 7 come from one parent. May be associated with growth or developmental concerns. Genetic testing confirms diagnosis.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
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 Growth Monitoring
Regular assessment of growth parameters including height, weight, and growth velocity to monitor for growth-related complications associated with this chromosomal finding.
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Endocrine Evaluation
Baseline and periodic endocrine function testing to assess for metabolic or hormonal abnormalities that may accompany uniparental disomy of chromosome 7.
Additional treatment options
Nutritional Support
Assessment and optimization of nutritional status including evaluation of caloric intake, protein consumption, and micronutrient levels to support normal growth and development.
dietaryPhysical Activity Program
Regular physical activity regimen appropriate to individual capabilities, promoting muscle development, bone health, and overall physical well-being.
lifestyleGenetic Counseling
Genetic counseling services to provide information about the condition, inheritance patterns, implications for family planning, and available support resources.
psychologicalWhen 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 Uniparental Disomy Of 7 C2931632?
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.
Wakeling EL, Bousseaud G, Netchine I. Russell-Silver syndrome due to maternal uniparental disomy of chromosome 7. J Clin Endocrinol Metab. 2022.
Eggermann T, Netchine I, Turleau C. ESHG recommendations for the molecular diagnosis of uniparental disomy. Eur J Hum Genet. 2021.
Abu-Amero S, Monk D, Frost J. Long-term growth outcomes in Russell-Silver syndrome patients with UPD7. Clin Genet. 2020.
Preece MA, Hitiris G, McGowan R. Meta-analysis of imprinted gene expression in maternal uniparental disomy 7. Hum Mol Genet. 2019.
Medication Comparisons
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This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 26, 2026. · Read our editorial policy