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Синдром мікродуплікації 5р13

ORPHA:329802· ICD-10 Q92.3· 5p13 microduplication syndrome

Визначення(English summary)

A rare partial autosomal trisomy/tetrasomy characterized by global developmental delay, intellectual disability, autistic behavior, muscular hypotonia, macrocephaly and facial dysmorphism (frontal bossing, short palpebral fissures, low set, dysplastic ears, short or shallow philtrum, high arched or narrow palate, micrognathia). Other associated clinical features include sleep disturbances, seizures, aplasia/hypoplasia of the corpus callosum, skeletal abnormalities (large hands and feet, long fingers and toes, talipes).

Поширеність
<1 / 1 000 000
Успадкування
Not applicable, Unknown
Вік початку
Infancy, Neonatal