A rare chromosomal anomaly syndrome with highly variable phenotype. Principal characteristics are intrauterine growth retardation, failure to thrive, developmental delay, hypotonia, mild dysmorphic features (including microcephaly, short forehead, up
syndrome du chromosome 2 en anneau
SNOMEDCT-BE (including microcephaly, short forehead, up / 765485000
SNOMEDCT-BE (disorder) / 765485000