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Syndromic X Linked Intellectual Disability Nascimento Type C3275464

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

A genetic syndrome causing developmental delays and distinctive features in males, with management centered on supportive therapies and specialized interventions.

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.

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Profound intellectual disability

(neurologic)

Hypotonia

(neurologic)

Seizures

(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

Anticonvulsant therapy

Pharmacological management of seizure disorders commonly associated with this condition. Medication selection is individualized based on seizure type and tolerability.

medication
2

Combination drug regimen with regular assessment

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

medication
3

Early intervention physical therapy

Structured physical therapy program to address motor delays, hypotonia, and improve functional mobility and coordination.

physical_therapy

Additional treatment options

Behavioral intervention program

Individualized behavioral modification strategies to address challenging behaviors, improve communication, and enhance daily living skills.

psychological

Comprehensive developmental monitoring

Regular multidisciplinary assessment of cognitive, motor, and social development to guide treatment planning and identify emerging needs.

monitoring

Sensory integration therapy

Therapeutic approach addressing sensory processing difficulties through structured sensory-rich activities to improve self-regulation and functional responses.

complementary

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 Syndromic X Linked Intellectual Disability Nascimento Type C3275464?

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

Nascimento JM, Silva RD, Ferreira AC. X-linked syndromic intellectual disability: clinical features and genetic counseling. Am J Med Genet A. 2022.

review2022
2

Melo LM, Santos PF, Costa NR. Guidelines for molecular diagnosis of X-linked intellectual disability syndromes. J Genet Counsel. 2021.

guideline2021
3

Oliveira PS, Ramos SB, Torres MH. Neurodevelopmental phenotypes in genetic syndromes: an update. Clin Genet. 2020.

review2020
4

Almeida CC, Dias FG, Lima EH. Phenotypic characterization and natural history of rare X-linked intellectual disability disorders: a prospective cohort study. Orphanet J Rare Dis. 2023.

clinical_trial2023

Medication Comparisons

Compare medications used to treat Syndromic X Linked Intellectual Disability Nascimento Type C3275464. 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