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Lymphedema praecox

From Wikipedia, the free encyclopedia
Lymphedema praecox
Other namesMeige disease Meige lymphedema[1]
Lymphedema praecox is inherited in an autosomal dominant manner
SpecialtyMedical genetics Edit this on Wikidata

Lymphedema praecox[2] is a condition characterized by swelling of the soft tissues in which an excessive amount of lymph has accumulated, and generally develops in females between the ages of nine and twenty-five. This is the most common form of primary lymphedema, accounting for about 80% of the patients.[3]: 848 [4]

See also

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References

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  1. ^ "Hereditary lymphedema type II | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 21 April 2019.
  2. ^ Sabiston 18 edition
  3. ^ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
  4. ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
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