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Brachydactyly Type A2 With Microcephaly C1859393

Published: July 22, 2026Updated: August 27, 2026

A genetic condition combining short fingers with an abnormally small head size. Developmental support and monitoring for associated concerns are important.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 27, 2026Editorial policy

Key facts at a glance

ICD-10
Q02
ICD-11
LA00.0
Body system
congenital
Severity
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(congenital)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Intellectual disability

(neurological)

Microcephaly

(neurological)

Short stature

(musculoskeletal)

Brachydactyly

(musculoskeletal)

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

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Neurodevelopmental surveillance

Regular monitoring of head growth, developmental milestones, and neurological status through pediatric neurology follow-up to identify any regression or emerging concerns early.

monitoring
3

Motor development intervention

Early intervention physical therapy to support gross and fine motor skill development, address muscle tone abnormalities, and promote age-appropriate motor milestones.

physical_therapy

Additional treatment options

Developmental psychology support

Comprehensive psychological assessment and ongoing support services to address learning difficulties, cognitive development, and behavioral concerns associated with microcephaly.

psychological

Family counseling and genetic education

Genetic counseling for families to understand the inheritance pattern and recurrence risks, combined with psychological support for coping with the diagnosis.

complementary

Growth and endocrine evaluation

Periodic assessment of growth parameters, endocrine function, and pubertal development to identify any associated hormonal deficiencies requiring intervention.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Brachydactyly Type A2 With Microcephaly C1859393?

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 Brachydactyly Type A2 With Microcephaly C1859393. 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 27, 2026. · Read our editorial policy