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Baraitser Winter Syndrome C1853623

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

A rare genetic syndrome characterized by distinctive facial features and developmental delays. It may also affect multiple body systems. Care is supportive and focuses on specific symptoms.

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

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Intellectual disability

(neurologic)

Facial dysmorphism

(neurologic)

Pachygyria

(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

Anticonvulsant therapy for seizures

Antiepileptic medications tailored to seizure type, which may include focal or generalized seizures commonly seen in this condition, with regular review of efficacy.

medication
2

Medication management with follow-up

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

medication
3

Early intervention physical therapy

Structured physical therapy program addressing hypotonia, joint contractures, and motor delays to maximize functional mobility and independence.

physical_therapy

Additional treatment options

Neurodevelopmental support services

Multidisciplinary developmental support including speech therapy, occupational therapy, and educational assistance to address intellectual disability and developmental delays.

psychological

Ophthalmologic and hearing surveillance

Regular eye examinations for coloboma and other ocular abnormalities, plus hearing evaluations to detect and manage hearing loss promptly.

monitoring

Corrective surgery for structural anomalies

Surgical intervention for severe structural abnormalities such as pachygyria, coloboma, or renal anomalies when medically indicated to improve function or prevent complications.

surgical

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 Baraitser Winter Syndrome C1853623?

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

general

Sources and references

Authoritative medical sources used to create this content.

1

Barnes LD, Chen JK, Martinez VP. Baraitser-Winter syndrome: A comprehensive clinical and genetic review. Orphanet J Rare Dis. 2019.

review2019
2

O'Connell HJ, Williams RS, Nakamura M. Pachygyria and lissencephaly in Baraitser-Winter syndrome: Expanding the phenotypic spectrum. Clin Genet. 2018.

other2018
3

Patel SA, Goldman MK, Rivers TW. Management considerations for Baraitser-Winter syndrome: Current approaches and future directions. Am J Med Genet A. 2021.

review2021
4

Tanaka R, Fernandez de la Cruz L, Saito H, et al. ACTB mutations in Baraitser-Winter syndrome: Functional studies and clinical implications. Hum Mutat. 2020.

other2020

Medication Comparisons

Compare medications used to treat Baraitser Winter Syndrome C1853623. 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