Article
A three-year follow-up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally.
Prenatal diagnosis - 1 Jan 1991
Camurri L, Chiesi A
Abstract excerpt
We report on a case of trisomy 8 mosaicism detected prenatally in a single clone of amniotic fluid culture, and confirmed on fetal blood and on peripheral lymphocytes after birth. A follow-up was performed over 3 years, showing a clinically normal female with cognitive, neuropsychological, and linguistic development in a normal range.
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