A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are a neonatal mewing cry, severe developmental delay and intellectual disability, short stature, hypotonia, dysmorphic features (including microcephaly,
syndrome du chromosome 5 en anneau
SNOMEDCT-BE (including microcephaly, / 765487008
SNOMEDCT-BE (disorder) / 765487008