Trisomy 9q Syndrome 757e45h 757e45h 757e45h 757e45h 757e45h 757e45h 1
General: Congenital mental retardation syndrome due to 9p trisomy.
Ocular: Hypertelorism; deep-set eyes; antimongoloid (up-slanting) eyes.
Clinical: Mental retardation; short stature; down-turned comers of the mouth; slightly or moderately bulbous nose; moderately large ears; nail dysplasia and hypoplasias; clinodactyly; abnormal dermatoglyphs.
Centerwall WR, Miller KS, Reeves LM. Familial 'partial 9q' trisomy: six cases and four carriers in three generations. J Med Genet 1976; 13:57-61.
Wahlstrom J, Gustavasson KH. Trisomy 9p syndrome in siblings. Clin Genet 1978; 13:511.
Young RS, et al. The dermatoglyphic and Clinical features of the 9p trisomy and partial 9p monosomy syndromes. Hum Genet 1985; 62:31-39.
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