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[戴格维-梅尔基奥尔-克劳森综合征:IV型黏多糖贮积症或莫尔基奥氏病的鉴别诊断]

[Dyggve-Melchior-Clausen syndrome: differential diagnosis of mucopolysaccharidosis type IV or Morquio disease].

作者信息

Coëslier A, Boute-Bénéjean O, Moerman A, Fron D, Manouvrier-Hanu S

机构信息

Service de génétique clinique, hôpital Jeanne-de-Flandre, centre hospitalier régional et universitaire de Lille, 2, avenue Oscar-Lambret, 59037 Lille, France.

出版信息

Arch Pediatr. 2001 Aug;8(8):838-42. doi: 10.1016/s0929-693x(01)00544-9.

Abstract

UNLABELLED

Dyggve-Melchior-Clausen syndrome (DMCS) is an autosomal recessive skeletal dysplasia. Clinical and radiological similarities with Morquio's syndrome can initially lead wrongly to this diagnosis.

CASE REPORT

A nine-year-old boy had mental retardation and progressive postnatal dwarfism. Platyspondyly and dysplastic epiphyses and metaphyses resembled those of Morquio's disease; however, clinical and radiological data led to the diagnosis of DMCS.

CONCLUSION

Clinical and paraclinical features allowing the differentiation of Morquio's syndrome and DMCS are discussed. Initial clinical presentation may be similar, but the intellectual prognosis is different.

摘要

未标注

迪格维-梅尔基奥尔-克劳森综合征(DMCS)是一种常染色体隐性遗传性骨骼发育不良。其与莫尔基奥综合征在临床和影像学上的相似性最初可能会导致误诊。

病例报告

一名9岁男孩有智力发育迟缓及出生后进行性侏儒症。扁平椎以及发育异常的骨骺和干骺端与莫尔基奥病相似;然而,临床和影像学资料最终诊断为DMCS。

结论

讨论了有助于区分莫尔基奥综合征和DMCS的临床及辅助检查特征。两者初始临床表现可能相似,但智力预后不同。

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