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Start free with EleplanX-linked intellectual disability, Nascimento type
ORPHA:163956Disease
Also called X-linked intellectual disability-nail dystrophy-seizures syndrome
What it is
X-linked intellectual disability, Nascimento type is a rare X-linked intellectual disability syndrome characterized by intellectual disability (with severe speech impairment), a myxedematous appearance, dysmorphic facial features (including large head, synophrys, prominent supraorbital ridges, almond-shaped and deep-set eyes, large ears, wide mouth with everted lower lip and downturned lip corners), low posterior hairline, short, broad neck, marked general hirsutism and abnormal hair whorls, skin changes (e.g. dry skin or hypopigmented spots), widely spaced nipples, obesity, micropenis, onychodystrophy and seizures.
Key facts
- Prevalence
- <1 / 1 000 000
- Age of onset
- Infancy
- Inheritance
- X-linked recessive
- Classified as
- Disease
Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.
Signs and symptoms
Common30–79%
24- Abnormal cerebral white matter morphology
- Aggressive behavior
- Broad neck
- Chronic constipation
- Depressed nasal bridge
- Downturned corners of mouth
- Echolalia
- Generalized hirsutism
- Hypertelorism
- Hypointensity of cerebral white matter on MRI
- Intellectual disability, severe
- Low posterior hairline
- Macrocephaly
- Micropenis
- Neonatal hyperbilirubinemia
- Pes cavus
- Seizure
- Short foot
- Synophrys
- Thin vermilion border
- Upslanted palpebral fissure
- Ventricular septal defect
- Vesicoureteral reflux
- Wide intermamillary distance
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
Gene
ICD-10 codes
ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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