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pro vyhledávání: '"Shohel Sarkar"'
Autor:
Faizul Islam Chowdhury, Shahimur Pervez, Matiur Rahman, Jayanta Banik, Shohel Sarkar, Ahmedul Kabir, Pinaki Paul
Publikováno v:
Journal of Medicine. 11:189-192
Milroy’s disease is an old term used to describe hereditary congenital lymphedema. It is the rarest of the inheritedlymphedema. The cause is a mutation in the VEGFR3 gene and is inherited in an autosomal dominant manner. Thisgene has been mapped to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec8d387d112bdb7244720b6f2732ed7
https://doi.org/10.3329/jom.v11i2.5471
https://doi.org/10.3329/jom.v11i2.5471
