The EuroBiotech Journal
MAGI group activity - Research, diagnosis and treatment of genetic and rare diseases
Data publikacji: 28 gru 2017
Zakres stron: 144 - 146
DOI: https://doi.org/10.24190/ISSN2564-615X/2017/S2.07
Słowa kluczowe
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This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.
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.