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A case of 18 trisomy syndrome in a female baby who bom at our K.V.H. was presented. The baby
had multiple anomalies those were characterized by intrauterine growth retardation, narrow microce-
phalic skull with prominent occiput, low-set malformed ears, micrognathia, rocker-bottom feet with
short & big toe, shield-like chest and webbed neck.
Chromosomal study showed trisomy 18.
On autopsy, Horseshoe-kidney had been found. |