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EPHB4 mutation causes adult and adolescent-onset primary lymphedema.

Arin K GreenePascal BrouillardChristopher L SudduthPatrick J SmitsDennis J KonczykMiikka Vikkula
Published in: American journal of medical genetics. Part A (2021)
Primary lymphedema results from the anomalous development of the lymphatic system and typically presents during infancy, childhood, or adolescence. Adult-onset primary lymphedema is rare and mutations associated with this condition have not been identified. The purpose of this investigation was to search for variants that cause adult-onset primary lymphedema. We discovered an autosomal dominant EPHB4 mutation in a patient who developed unilateral leg lymphedema at age 39 years; the same mutation affected his son who presented with the disease at 14 years of age.
Keyphrases
  • young adults
  • mental health
  • depressive symptoms
  • case report
  • gene expression
  • body mass index
  • copy number