Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Congenital nervous system disorder · Developmental disability · Congenital limb malformation · Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Congenital radioulnar synostosis
Radioulnar synostosis-developmental delay-hypotonia syndrome
Radioulnar synostosis-developmental delay-hypotonia syndrome, also known as Der Kaloustian-McIntosh-Silver syndrome, is an extremely rare syndrome with synostosis described in about 4 patients to date with clinical manifestations including congenital unilateral radioulnar synostosis, generalized hypotonia, developmental delay, and dysmorphic facial features (long face, prominent nose and ears).
This condition has no sub-types.