Trisomy 17p Syndrome 1
General: Trisomy 17p duplicatio 616f52g n syndrome.
Ocular: Hypertelorism, antimongoloid (up-slanting) palpebral fissures.
Clinical: Growth retardation; microcephaly; long philtrum with a thin upper lip; micrognathia; high-arched palate.
Schrander-Stumpel C, et al. Trisomy 17p due to a t(8;17) (p23;p11.2)pat translocation. Case report and review of the literature. Clin Genet 1990; 37:148-l52.
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