PEN-HUA SU2026-10-162026-10-162011-10-01Pure ID: 15412176Pure UUID: ec010f33-5209-4d63-992c-3a4c2a0d69d210.1016/j.pedneo.2011.06.008https://www.scopus.com/pages/publications/80055069773https://scholars.csmu.edu.tw/handle/123456789/33676We describe two siblings with generalized hypotonia, expressive language delay, developmental delay, mild facial dysmorphism, and accelerated growth. In addition, the male sibling had testis dysgenesis. Cytogenetic evaluation revealed an unbalanced maternally inherited translocation t(15;22)(q26;q13.3) resulting in partial monosomy 22q and trisomy 15q. The combination of deletion 22q and duplication 15q has not been described previously.3enjournal article