Galloway Mowat Syndrome 1 C4551772
A rare genetic syndrome causing kidney disease and brain abnormalities. Presents in infancy with poor growth and requires supportive care for symptoms.
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
Seizures
Generalized symptoms
(neurologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Microcephaly
(neurologic)Developmental delay
(neurologic)Ataxia
(neurologic)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
Drug therapy and clinical monitoring
Active treatment with regular monitoring by a healthcare provider is recommended.
Immunosuppressive therapy for nephrotic syndrome
Corticosteroids and other immunosuppressants are used to manage kidney involvement and reduce proteinuria in Galloway-Mowat syndrome.
Regular renal function monitoring
Frequent assessment of kidney function through blood tests, urine analysis, and blood pressure monitoring to detect deterioration early.
Additional treatment options
Renal-friendly nutritional support
Customized diet to manage protein restriction, sodium control, and appropriate calorie intake to support kidney function and overall growth.
dietarySeizure management interventions
Surgical evaluation and intervention for refractory seizures including possible vagus nerve stimulation when anticonvulsant medications fail.
surgicalNeurodevelopmental support services
Early intervention programs and psychological support addressing cognitive delays, motor skill development, and family counseling needs.
psychologicalWhen 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 Galloway Mowat Syndrome 1 C4551772?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalMedication Comparisons
Compare medications used to treat Galloway Mowat Syndrome 1 C4551772. 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.
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 25, 2026. · Read our editorial policy