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Milroy disease

Orpha number ORPHA79452
Synonym(s) Hereditary lymphedema type I
Nonne-Milroy lymphedema
Prevalence Unknown
Inheritance Autosomal dominant
Age of onset Infancy
Neonatal
ICD-10
  • Q82.0
ICD-O -
OMIM
UMLS
  • C1704423
MeSH -
MedDRA -

Summary

Milroy disease is a frequent form of primary lymphedema (see this term) characterized generally by painless, chronic lower-limb lymphedema found at birth or developing in the early neonatal period.


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Detailed information

Article for general public
  • FR (2007,pdf)
Clinical genetics review
  • EN (2009)
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