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

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

Abstract

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.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Bone Diseases, Developmental / congenital
  • Bone Diseases, Developmental / diagnosis*
  • Child
  • Diagnosis, Differential
  • Dwarfism / etiology*
  • Humans
  • Intellectual Disability / etiology*
  • Male
  • Mucopolysaccharidosis IV / diagnosis*
  • Syndrome