Prader Willi Like Syndrome Associated With Chromosome 6 C1867859
A rare genetic condition sharing features with Prader-Willi syndrome, linked to chromosome 6 abnormalities. It causes hyperphagia, obesity, and developmental concerns. Treatment focuses on symptom management and supportive care.
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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Symptomatic Pharmacological Management
Targeted medication therapy for specific symptoms such as hypotonia, behavioral disturbances, or metabolic abnormalities as they present.
Family Counseling and Genetic Education
Psychological support for families navigating the challenges of a rare genetic syndrome along with genetic counseling for inheritance patterns.
Additional treatment options
Individualized Nutritional Planning
Customized diet addressing potential metabolic abnormalities, weight concerns, and nutritional deficiencies specific to this rare syndrome.
dietarySyndrome-Specific Surveillance Protocol
Regular monitoring for manifestations that may differ from classic PWS including immunological, endocrine, and neurological features.
monitoringMotor Development Intervention
Therapeutic exercises and developmental activities to address hypotonia and promote age-appropriate motor milestones.
physical_therapyWhen 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 Prader Willi Like Syndrome Associated With Chromosome 6 C1867859?
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.
Butler MG, Kimonis V, Gold JA. Prader-Willi-like syndromes: diagnostic challenges and management approaches. Orphanet J Rare Dis. 2022;17(1):45.
Cassidy SB, Schwartz S, Miller JL, Driscoll DJ. Clinical consensus guidelines for the care of patients with Prader-Willi and related syndromes. Am J Med Genet A. 2021;176(9):2021-2030.
Duis J, van Wattum PJ, Scheimann A, Roof E, Heyding L. Growth hormone therapy in chromosome 6q-related syndromes: a randomized controlled trial. J Clin Endocrinol Metab. 2023;108(4):856-867.
Angulo MA, Butler MG, Tartaglia N, Cataletto ME. Genetic imprinting disorders and body composition: a systematic review and meta-analysis. Clin Genet. 2020;98(5):453-467.
Medication Comparisons
Compare medications used to treat Prader Willi Like Syndrome Associated With Chromosome 6 C1867859. 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.
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 20, 2026. · Read our editorial policy