Skeletal Changes in the «Cri du Chat» Syndrome

Author:

Dallapiccola B.,Pistocchi G.,Forabosco A.,Capra L.

Abstract

SummaryA radiological investigation was carried out in a group of patients with the “cri du chat” syndrome. The most striking skeletal abnormalities associated with the 5p- chromosome anomaly include microcephaly hypertelorism, narrowing of the wings of ilia, which often appear rectangular in shape. In older patients additional consistent radiological features include large frontal sinuses, malocclusions, scoliosis, shortness of some metacarpal and metatarsal bones. The radiological investigations in the “cri du chat” syndrome, although of small diagnostic aid, appear to be useful for a detailed characterization of the malformations.

Publisher

Cambridge University Press (CUP)

Reference3 articles.

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Craniofacial characteristics in cri-du-chat syndrome;Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology;2010-12

2. Cri du Chat syndrome;Orphanet Journal of Rare Diseases;2006-09-05

3. The natural history of Cri du Chat Syndrome. A report from the Italian Register;European Journal of Medical Genetics;2006-09

4. Progressive Scoliosis in Cri-Du-Chat Syndrome Over a 20-Year Follow-Up Period;Spine;2001-04

5. Studies of the cranial base in 23 patients with cri‐du‐chat syndrome suggest a cranial developmental field involved in the condition;American Journal of Medical Genetics;1999-01

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