Severien C, Felix S, Bartholomé K
Universitäts-Kinderklinik, St. Josef-Hospital Bochum.
Klin Padiatr. 1991 Nov-Dec;203(6):467-9. doi: 10.1055/s-2007-1025476.
A three year old girl with ring chromosome 22 is described. The clinical findings include epicanthus, flat nasal bridge, hypertelorism, long eye-lashes, lymphoedema, hypoplastic toe nails, hydrocephalus and muscular hypotonia. Speech and language development is delayed. At three years the child begins to walk.