We report on partial dup(22q), growth deficiency, and the facioauricul
overtebral sequence including hemifacial microsomia, cleft lip and pal
ate, preauricular tags, and hearing loss in one patient. No endocrine
or systemic cause for growth deficiency was identified. The case illus
trates applicability of chromosome analysis in syndrome-associated gro
wth failure, and a previously unreported associated chromosome abnorma
lity. (C) 1998 Wiley-Liss, Inc.