Morquio syndrome

Changed by Daniel J Bell, 15 Apr 2024
Disclosures - updated 22 Aug 2023: Nothing to disclose

Updates to Article Attributes

Body was changed:

Morquio syndrome (in older literature it is sometimes called Morquio-Brailsford syndrome) is an autosomal recessive mucopolysaccharidosis (MPS) type IV.

Epidemiology

Incidence estimated at ~1:40,000.

Clinical presentation

Many cases present at ~2 years of age and have normal intelligence. Clinical features:

  • severe dwarfism (<4 foot)

  • joint laxity

  • corneal opacification/clouding

  • lymphadenopathy

  • progressive deafness

  • spinal kyphoscoliosis

  • prominent mandible and lower face 

  • short neck

Pathology

It results from an excess of keratan sulphate due to a deficit in its degradation pathway. Keratan sulphate accumulates in various tissues inclusive of cartilage, the nucleus pulposus of the intervertebral discs and corneas.

Radiographic features

Plain radiograph / CT
Axial manifestations
Calvarial manifestations
Peripheral musculoskeletal manifestations
  • short and wide tubular bones

  • metaphyseal flaring in long bones

  • multiple epiphyseal centres

  • wide metacarpals with proximal pointing of index to little finger

  • irregular carpal bones 

  • flattened proximal femoral epiphyses; risk of lateral subluxation and dislocation

  • coxa valga

  • genu valgum

Thoracic manifestations
  • anterior sternal bowing, increased AP chest diameter, wide ribs

Echocardiography

Treatment and prognosis

Life expectancy ranges between 30-40 years. The most common cause of death is cervical myelopathy from C2 abnormality. Patients are also particularly vulnerable to respiratory infection.

History and etymology

Named after Luis Morquio, an Uruguayan paediatrician (1867-1935) published his first case in 1929 5. James Brailsford (1889-1961) 6 a renowned British radiologist made an important contribution to the understanding of the radiographic appearances of this condition, and also published his first case in 1929, independently of Morquio 8.

  • -</ul><h6>Thoracic manifestations</h6><ul><li><p>anterior sternal bowing, increased AP chest diameter, wide ribs</p></li></ul><h5>Echocardiography</h5><ul><li><p>late-onset <a href="/articles/aortic-valve-regurgitation">aortic regurgitation</a></p></li></ul><h4>Treatment and prognosis</h4><p>Life expectancy ranges between 30-40 years. The most common cause of death is cervical <a href="/articles/compressive-myelopathy">myelopathy</a> from C2 abnormality. Patients are also particularly vulnerable to respiratory infection.</p><h4>History and etymology</h4><p>Named after <strong>Luis Morquio</strong>, an Uruguayan paediatrician (1867-1935) <sup>5</sup>. <strong>James Brailsford </strong>(1889-1961) <sup>6</sup> a renowned British radiologist made an important contribution to the understanding of the radiographic appearances of this condition.</p>
  • +</ul><h6>Thoracic manifestations</h6><ul><li><p>anterior sternal bowing, increased AP chest diameter, wide ribs</p></li></ul><h5>Echocardiography</h5><ul><li><p>late-onset <a href="/articles/aortic-valve-regurgitation">aortic regurgitation</a></p></li></ul><h4>Treatment and prognosis</h4><p>Life expectancy ranges between 30-40 years. The most common cause of death is cervical <a href="/articles/compressive-myelopathy">myelopathy</a> from C2 abnormality. Patients are also particularly vulnerable to respiratory infection.</p><h4>History and etymology</h4><p>Named after <strong>Luis Morquio</strong>, an Uruguayan paediatrician (1867-1935) published his first case in 1929 <sup>5</sup>. <strong>James Brailsford </strong>(1889-1961) <sup>6</sup> a renowned British radiologist made an important contribution to the understanding of the radiographic appearances of this condition, and also published his first case in 1929, independently of Morquio <sup>8</sup>.</p>

References changed:

  • 8. Ellman P. Morquio-Brailsford's Disease Simulating the Arthritic Manifestation of Rheumatoid Disease. Ann Rheum Dis. 1949;8(4):267-76. <a href="https://doi.org/10.1136/ard.8.4.267">doi:10.1136/ard.8.4.267</a> - <a href="https://www.ncbi.nlm.nih.gov/pubmed/18623824">Pubmed</a>

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