Literature DB >> 17195803

The musculoskeletal manifestations of the Coffin-Lowry syndrome.

Jose A Herrera-Soto1, Alberto Santiago-Cornier, Lee S Segal, Norman Ramirez, Junichi Tamai.   

Abstract

Coffin-Lowry syndrome (CLS) is a rare genetic disorder characterized by craniofacial abnormalities, mental retardation, short stature, and hypotonia. Patients with CLS may present with multiple musculoskeletal abnormalities. The purpose of this study was to identify and characterize the musculoskeletal findings in 10 patients with CLS. Eight patients presented with thoracolumbar kyphosis or kyphoscoliosis, with a mean Cobb angle of 45 degrees in the coronal plane and 31 degrees of thoracolumbar kyphosis. These may be progressive and difficult to treat, needing early surgical treatment. Close follow-up of the spinal deformities is strongly recommended to document progression. Sixty percent of the patients presented with bilateral flexible and painless planovalgus deformities. Hypoplasia of the ilium and hand deformities are common but do not seem to cause any functional problems. Observation is recommended for these asymptomatic hand, foot, and pelvic findings.

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Year:  2007        PMID: 17195803     DOI: 10.1097/01.bpo.0000187994.94515.9d

Source DB:  PubMed          Journal:  J Pediatr Orthop        ISSN: 0271-6798            Impact factor:   2.324


  3 in total

1.  Eight years of follow-up after laminectomy of calcium pyrophosphate crystal deposition in the cervical yellow ligament of patient with Coffin-Lowry syndrome: A case report.

Authors:  Tadao Morino; Tadanori Ogata; Hideki Horiuchi; Shintaro Yamaoka; Mitsumasa Fukuda; Hiromasa Miura
Journal:  Medicine (Baltimore)       Date:  2016-08       Impact factor: 1.889

2.  Growth Concerns in Coffin-Lowry Syndrome: A Case Report and Literature Review.

Authors:  Ying Lv; Liuyan Zhu; Jing Zheng; Dingwen Wu; Jie Shao
Journal:  Front Pediatr       Date:  2019-01-25       Impact factor: 3.418

3.  The natural history of spinal deformity in patients with Coffin-Lowry syndrome.

Authors:  M Welborn; S Farrell; P Knott; E Mayekar; S Mardjetko
Journal:  J Child Orthop       Date:  2018-02-01       Impact factor: 1.548

  3 in total

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