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Title: Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy. Author: Gibbons B, Tan SY, Tam PY. Journal: Singapore Med J; 1999 Apr; 40(4):273-5. PubMed ID: 10487083. Abstract: We describe a 7-year-old boy presenting with mental retardation and hyperactivity. Clinical features include microcephaly, hypertelorism, epicanthic eye folds and antimongoloid slant. He also has large ears, large hands and feet, and torticollis. The karyotype was 46, XY, r (22) (p13q13). In situ hybridisation studies with a subtelomeric probe for distal 22q confirmed that the ring was deleted causing partial monosomy of 22q.[Abstract] [Full Text] [Related] [New Search]