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Синдром мікроделеції 9q21.13

ORPHA:531151· ICD-10 Q93.5· 9q21.13 microdeletion syndrome

Визначення(English summary)

A rare, genetic, intellectual disability malformation syndrome characterized by global developmental delay, intellectual disability, delayed speech and language development, epilepsy, autistic behavior, and moderate facial dysmorphism (including elongated face, narrow forehead, arched eyebrows, horizontal palpebral fissures, hypertelorism, epicanthus, midface flattening, short nose, long and featureless philtrum, thin upper lip, macrostomia, and prominent chin). Additional variable manifestations include microcephaly, hypotonia, hypertrichosis, and strabismus.

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