| Literature DB >> 15832359 |
Toshiyuki Yamamoto1, Kenji Kurosawa, Mitsuo Masuno, Shigeharu Okuzumi, Soichi Kondo, Sahoko Miyama, Nobuhiko Okamoto, Noriko Aida, Gen Nishimura.
Abstract
Rubinstein-Taybi syndrome (RTS; MIM# 180849) is a well-known malformation syndrome, characterized by broad thumbs and halluces, a characteristic facies, short stature, and mental retardation. RTS is accompanied by a variety of morbid complications, particularly of the skeleton. Based on the experience of five RTS patients with malformation of the craniovertebral junction, we draw attention to previously unrecognized life-threatening complications of RTS, including instability of C1-C2, os odontoideum, hypoplasia of the dens, and fusion of the cervical vertebrae. One patient developed severe cervical myelopathy. Malformation of the cervical spine may be a common syndromic constituent of RTS, to which special attention should be paid to prevent its neurologic sequelae. Copyright (c) 2005 Wiley-Liss, Inc.Entities:
Mesh:
Year: 2005 PMID: 15832359 DOI: 10.1002/ajmg.a.30708
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802