We report an 18 month old girl with developmental delay, dysmorphic features, and a karyotype 46,XX,del (1) (p32. lp32.3). To our knowledge the clinical features associated with this deletion have not been reported previously. (J Med Genet 1995;32:636-637) Chromosomal abnormalities involving lp are rare. We report the smallest deletion yet described, in a girl with developmental delay and multiple dysmorphic features.
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