Galloway Mowat Syndrome 8 C5193045
A genetic syndrome that impacts brain and kidney function. Usually identified in early childhood with developmental and kidney concerns. Management involves supportive treatments.
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.
Generalized symptoms
(neurologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Spastic tetraplegia
(neurologic)Severe developmental delay
(neurologic)Renal dysfunction
(neurologic)Ophthalmic abnormalities
(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
Growth and Development Assessment
Serial measurements of growth parameters, developmental milestones, and nutritional status to identify deficits early and guide intervention strategies.
Targeted drug therapy with dose adjustment
Active treatment with regular monitoring by a healthcare provider is recommended.
High-Calorie Nutritional Supplementation
Calorie-dense nutrition and supplementation to address failure to thrive and support adequate growth, often requiring nasogastric or gastrostomy feeds in severe cases.
Additional treatment options
Gastrostomy Tube Placement
Surgical feeding tube placement when oral intake is insufficient for nutritional needs, providing reliable route for nutrition and medication administration.
procedureEdema Management
Diuretic therapy and supportive measures to manage fluid retention associated with nephrotic syndrome, monitored carefully to avoid dehydration or electrolyte imbalance.
medicationGentle Complementary Therapies
Supportive complementary approaches such as therapeutic touch, music therapy, and aromatherapy to enhance comfort and quality of life for patients with severe illness.
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 Galloway Mowat Syndrome 8 C5193045?
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 8 C5193045. 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 20, 2026. · Read our editorial policy