Hennekam syndrome: a rare cause of primary lymphedema

Autor: Imane Elmansour, Soumia Chiheb, Hakima Benchikhi

Publikováno v: Elmansour, Imane; Chiheb, Soumia; & Benchikhi, Hakima. (2014). Hennekam syndrome: a rare cause of primary lymphedema. Dermatology Online Journal, 20(8). Retrieved from: http://www.escholarship.org/uc/item/4xk755pd

Hennekam syndrome (HS) is an autosomal recessive disorder characterized by the association of lymphedema, intestinal lymphangiectasia, moderate mental retardation, and facial dysmorphism. We describe a 14-year-old girl affected with Hennekam syndrome

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb67f912993d8762e044be1b7b837406
https://doi.org/10.5070/d3208023543