Galloway Mowat Syndrome 6 C5193043
A rare genetic syndrome causing kidney disease and brain abnormalities. Managed with supportive care targeting kidney and neurological 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
Hydrocephalus
Generalized symptoms
(neurologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Severe intellectual disability
(neurologic)Microcephaly
(neurologic)Peripheral neuropathy
(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.
Renal Function Surveillance
Systematic tracking of kidney parameters including proteinuria levels, serum creatinine, and estimated glomerular filtration rate to detect deterioration early and adjust interventions accordingly.
Proteinuria Control Therapy
Use of renoprotective agents to reduce protein loss through the kidneys and slow progressive renal disease, with regular monitoring for treatment efficacy and side effects.
Additional treatment options
Protein-Restricted Renal Diet
Carefully calculated protein intake to minimize kidney workload while meeting growth and maintenance needs, often combined with phosphorus and potassium management.
dietaryVP Shunt Placement if Hydrocephalus Present
Surgical intervention for cerebrospinal fluid shunting when hydrocephalus develops, requiring careful evaluation given the underlying neurological abnormalities in Galloway-Mowat syndrome.
surgicalIntegrative Supportive Care
Complementary approaches including massage therapy, gentle movement practices, and stress-reduction techniques to improve quality of life and support overall wellbeing alongside conventional treatments.
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 6 C5193043?
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 6 C5193043. 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