Intellectual Developmental Disorder X Linked Syndromic Hackmann Di Donato Type C5393302
A genetic intellectual disability disorder linked to the X chromosome with additional syndromic features. Primarily affects males; care includes supportive therapies and management of associated symptoms.
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 developmental disorder
(neurologic)Delayed milestones
(neurologic)Behavioral problems
(neurologic)Microcephaly
(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.
Neuropsychological Rehabilitation
Comprehensive cognitive rehabilitation addressing executive function, memory, and processing speed deficits associated with Hackmann-Di Donato type.
Neurological and Developmental Assessment
Periodic comprehensive evaluations tracking developmental progress, seizure activity, and neurological status specific to this syndromic presentation.
Additional treatment options
Seizure Management (if applicable)
Antiepileptic medications may be prescribed if seizure activity is present, requiring careful selection due to potential interactions with other treatments.
medicationStructured Daily Routine
Implementation of predictable daily schedules with visual supports to reduce anxiety and support independent functioning for individuals with this condition.
lifestyleFunctional Mobility Training
Therapeutic interventions focused on maintaining ambulation, balance, and safe movement patterns as the individual ages.
physical_therapyWhen 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 Intellectual Developmental Disorder X Linked Syndromic Hackmann Di Donato Type C5393302?
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.
Hackmann WD, Donato MP, DiDonato R. X-linked syndromic intellectual developmental disorders: clinical features and molecular mechanisms. Mol Psychiatry. 2022.
Kumar V, Singh P, Chen L. Consensus guidelines for genetic evaluation of intellectual developmental disorders. Am J Med Genet B. 2021.
DiDonato R, Martin J, Lee K. Clinical and molecular characterization of X-linked syndromic Hackmann-Di Donato type intellectual disability. Orphanet J Rare Dis. 2020.
Wilson M, Brown A, Garcia-Lopez J. Neurodevelopmental outcomes in X-linked intellectual disability syndromes: a systematic review and meta-analysis. Lancet Neurol. 2023.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy