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Hyaluronidase deficiency
from Wikipedia
Hyaluronidase deficiency
Other namesMucopolysaccharidosis type IX
Structure of HYAL-1
SpecialtyDermatology
Symptomsshort stature, mildly dysmorphic facial features, soft tissue masses, knee and hip pain
Usual onsetChildhood
CausesDeficiency of the enzyme hyaluronidase
Frequencyless than 1 in 1,000,000

Hyaluronidase deficiency, also known as Mucopolysaccharidosis type IX or MPS IX, is a condition caused by mutations in the HYAL1 gene, and is characterized by multiple soft-tissue masses.[1]: 544 

Signs and symptoms

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As hyaluronidase deficiency is an extremely rare disorder, a clear clinical picture of the disease has not been formed. However, the following symptoms may occur:[2]

  • Multiple soft tissue masses which may experience temporary episodes of painful swelling.
  • Temporary episodes of generalized cutaneous swelling.
  • Frequent episodes of otitis media.
  • Short stature.
  • Mildy dysmorphic facial features such as a flattened nasal bridge, a bifid (split) uvula, and a submucosal cleft palate.
  • Joint movement and intellectual ability are unaffected.[3]

Diagnosis

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It is diagnosed through a combination of a thorough clinical evaluation in which characteristic findings are identified, specialized tests that can detect things like excessive levels of mucopolysaccharides and enzym essays to see if there is a deficiency in the enzyme hyaluronidase.[4]

Treatment

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At the moment, there are no effective treatments against hyaluronidase deficiency. The only treatment possible is symptomatic and meant to manage and alleviate individual symptoms.[5]

See also

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References

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Further reading

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