Trisomy 8p

Orpha code: 264450OMIM code:

Definition

Trisomy 8p is a rare chromosomal anomaly syndrome, resulting from the partial duplication of the short arm of chromosome 8, with highly variable phenotype ranging from no dysmorphic features and only mild intellectual disability to patients with severe developmental delay, neonatal hypotonia, short stature, profound intellectual disability, mild dysmorphic features (e.g. mild ptosis, hypertelorism, down-slanting palpebral fissures, broad nasal bridge, short, prominent philtrum, abnormal dentition) and structural brain abnormalities. Autism, epilepsy, and spastic paraplegia have also been reported.

Disease data
Classification

Malformation syndrome

Synonyms
Duplication 8p
Duplikacja 8p
ORPHA code
264450
OMIM code
-
ICD10 code
Q92.2
ICD11 code
-

No additional description.

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