Morquio syndrome

Last revised by Arlene Campos on 7 Nov 2024

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

Incidence is estimated at ~1:40,000.

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

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.

  • short and wide tubular bones

  • metaphyseal flaring in long bones

  • multiple epiphyseal centers

  • 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

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

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.

Named after Luis Morquio, an Uruguayan pediatrician (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.

Cases and figures

  • Case 1: showing wide proximal pointing metacarpals
  • Case 2
  • Case 3: diffuse platyspondyly
  • Case 4: mucopolysaccharidoses
  • Case 5: anterior central vertebral body beaking
  • Case 6
:

Updating… Please wait.

 Unable to process the form. Check for errors and try again.

 Thank you for updating your details.