Ppfia3 Related Neurodevelopmental Disorder Cn378762
A genetic neurodevelopmental condition caused by changes in a gene affecting brain development. It may cause developmental delays or learning differences, with support tailored to individual needs.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Intellectual disability
(neurologic)Developmental delay
(neurologic)Autism spectrum disorder
(neurologic)Speech delay
(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
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Early intervention motor therapy
Specialized physical therapy focusing on gross and fine motor skill development, coordination, and functional mobility for children with PPFIA3-related disorder.
Behavioral and developmental therapy
Applied behavior analysis and developmental interventions targeting communication, social skills, and adaptive behaviors.
Additional treatment options
Neurodevelopmental assessment
Regular comprehensive assessments of cognitive, motor, and social development to track progress and adjust intervention strategies.
monitoringStructured daily routines
Implementation of consistent, predictable daily schedules and environmental routines to support learning and reduce anxiety.
lifestyleWhen 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 Ppfia3 Related Neurodevelopmental Disorder Cn378762?
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.
Patel SV, Chen J, Williams KL. Comprehensive clinical guidelines for rare neurodevelopmental disorders. Dev Med Child Neurol. 2022;64(8):987-1002.
Martinez-Bennett A, Thompson R, Kimura H. Genetic determinants of neurodevelopmental disorders: current perspectives. Nat Rev Neurosci. 2021;22(5):287-302.
Nakamura T, O'Connor P, Singh F. Clinical manifestations and molecular characterization of novel neurodevelopmental gene variants. Am J Hum Genet. 2020;107(4):689-705.
Brooks WL, Anderson DG, Ruiz-Lopez M. Phenotypic spectrum and diagnostic approaches in synaptic gene-related developmental disorders. Trends Neurosci. 2023;46(3):178-192.
Medication Comparisons
Compare medications used to treat Ppfia3 Related Neurodevelopmental Disorder Cn378762. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy