The EuroBiotech Journal
MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
À propos de cet article
Publié en ligne: 28 déc. 2017
Pages: 144 - 146
DOI: https://doi.org/10.24190/ISSN2564-615X/2017/S2.07
Mots clés
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Primary lymphedema can be familial (in which more than one member of the same family has a lymphedema phenotype), syndromic (in which lymphedema is one symptom of a complex clinical syndrome) or sporadic (in which an isolated family member has lymphedema). All types of lymphedema are determined by genetic alteration of one or more genes. Not all the genes involved are known.