Morquio syndrome

Changed by Mostafa Elfeky, 1 Jan 2024
Disclosures - updated 14 May 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 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 Keratan sulphate accumulates in various tissues inclusive of cartilage, the nucleus pulposus of the intervertebral discs and 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) 5. James Brailsford (1889-1961) 6 a renowned British radiologist made an important contribution to the understanding of the radiographic appearances of this condition.

  • -<p><strong>Morquio syndrome</strong> (in older literature it is sometimes called <strong>Morquio-Brailsford syndrome</strong>) is an autosomal recessive <a href="/articles/mucopolysaccharidoses-2">mucopolysaccharidosis (MPS)</a> type IV.</p><h4>Epidemiology</h4><p>Incidence estimated at ~1:40,000.</p><h4>Clinical presentation</h4><p>Many cases present at ~2 years of age and have normal intelligence. Clinical features:</p><ul>
  • +<p><strong>Morquio syndrome</strong>&nbsp;(in older literature it is sometimes called <strong>Morquio-Brailsford syndrome</strong>) is an autosomal recessive <a href="/articles/mucopolysaccharidoses-2">mucopolysaccharidosis (MPS)</a>&nbsp;type IV.</p><h4>Epidemiology</h4><p>Incidence estimated at ~1:40,000.</p><h4>Clinical presentation</h4><p>Many cases present at ~2 years of age and have normal intelligence. Clinical features:</p><ul>
  • -<li><p>prominent mandible and lower face </p></li>
  • +<li><p>prominent mandible and lower face&nbsp;</p></li>
  • -</ul><h4>Pathology</h4><p>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 <a href="/articles/nucleus-pulposus">nucleus pulposus</a> of the <a href="/articles/intervertebral-disc">intervertebral discs</a> and corneas.</p><h4>Radiographic features</h4><h5>Plain radiograph / CT</h5><h6>Axial manifestations</h6><ul>
  • +</ul><h4>Pathology</h4><p>It results from an excess of keratan sulphate due to a deficit in its degradation pathway.&nbsp;Keratan sulphate accumulates in various tissues inclusive of cartilage, the <a href="/articles/nucleus-pulposus">nucleus pulposus</a> of the <a href="/articles/intervertebral-disc">intervertebral discs</a>&nbsp;and corneas.</p><h4>Radiographic features</h4><h5>Plain radiograph / CT</h5><h6>Axial manifestations</h6><ul>
  • -<li><p>posterior vertebral body scalloping</p></li>
  • -<li><p>round vertebral bodies </p></li>
  • +<li><p><a href="/articles/vertebral-scalloping" title="Vertebral body scalloping">posterior vertebral body scalloping</a></p></li>
  • +<li><p>round vertebral bodies&nbsp;</p></li>
  • -<li><p>goblet shaped flared iliac wings, increased acetabular angles and constricted iliac bone base</p></li>
  • +<li><p>goblet shaped flared iliac wings, increased <a href="/articles/acetabular-angle" title="Acetabular angle">acetabular angles</a> and constricted iliac bone base</p></li>
  • -<li><p>irregular <a href="/articles/carpal-bones">carpal bones</a> </p></li>
  • +<li><p>irregular <a href="/articles/carpal-bones">carpal bones</a>&nbsp;</p></li>

References changed:

  • 4. Peter Beighton. McKusick's Heritable Disorders of Connective Tissue. (1993) ISBN: 9780801663581 - <a href="http://books.google.com/books?vid=ISBN9780801663581">Google Books</a>
  • 4. Blighton D. Heritable disorders of connective tissue, 5th ed. St. Louis: CV Mosby; 1993.

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