论文信息 - A three‐year follow‐up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally

A three‐year follow‐up on a child with low level trisomy 8 mosaicism which was diagnosed prenatally

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.

L. Camurri | A. Chiesi | Annalisa Chiesi

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