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Hao Fountain Syndrome Due To 16p13 2 Microdeletion C5680086

Published: July 22, 2026Updated: August 25, 2026

A neurodevelopmental disorder from a small chromosomal deletion causing developmental delay, distinctive facial features, and often intellectual disability. Treatment involves multidisciplinary supportive care.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

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

Developmental delay

(neurologic)

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(neurologic)

Facial dysmorphism

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Early Intensive Developmental Therapy

Multidisciplinary early intervention focusing on motor skills, communication, and cognitive development tailored to neurodevelopmental needs.

physical_therapy
2

Targeted drug therapy with dose adjustment

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Specialized Educational Support

Individualized education plans with appropriate accommodations, learning strategies, and behavioral interventions for academic success.

psychological

Additional treatment options

Speech and Communication Therapy

Augmentative and alternative communication support including sign language, picture exchange systems, and speech-generating devices.

complementary

Growth and Development Surveillance

Regular pediatric monitoring of growth parameters, developmental milestones, and identification of associated medical conditions.

monitoring

Family Support and Counseling

Psychosocial support for parents and caregivers addressing stress management, resource navigation, and family resilience building.

psychological

When 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.

Q

What is Hao Fountain Syndrome Due To 16p13 2 Microdeletion C5680086?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Hao Fountain Syndrome Due To 16p13 2 Microdeletion C5680086. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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