Katsantoni Papadakou Lagoyanni Syndrome C2931394
A rare genetic syndrome characterized by multiple organ system abnormalities. It is present from birth and requires multidisciplinary care. Management focuses on addressing specific symptoms and providing supportive therapies.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Epileptic seizures
Generalized symptoms
(neurologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Developmental delay
(neurologic)Muscle hypotonia
(neurologic)Feeding difficulties
(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
Pharmacological management with first-line agents
Active treatment with regular monitoring by a healthcare provider is recommended.
Syndrome-specific surveillance program
Regular monitoring of known organ system involvement including cardiac, renal, and neurological assessments at recommended intervals.
Anomaly-directed surgical care
Surgical management of structural abnormalities when medically indicated, including cardiac surgery, orthopedic procedures, or genitourinary reconstruction.
Additional treatment options
Motor development support
Early intervention physical therapy to address developmental delays, improve gross motor skills, and prevent secondary musculoskeletal complications.
physical_therapyNutritional support and feeding management
Assessment and management of feeding difficulties, nutritional deficiencies, and weight concerns common in this population through specialized dietary planning.
dietaryIntegrative supportive therapies
Adjunctive therapies such as occupational therapy, speech therapy, and complementary approaches to address communication, fine motor, and sensory needs.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
See a doctor within 24 hours
Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.
Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.
Frequently asked questions
Common questions about this topic.
What is Katsantoni Papadakou Lagoyanni Syndrome C2931394?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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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.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy