Familial Partial Lipodystrophy: Clinical Features, Genetics and Treatment in a Greek Referral Center

Familial partial lipodystrophy (FPLD) is a rare syndrome in which a patient’s phenotype is not merely dependent on the specific genetic mutation, but it is also defined by a combination of other demographic, environmental and genetic factors. In this prospective observational study in a Greek referr...

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Detalles Bibliográficos
Autores principales: Kountouri, Aikaterini, Korakas, Emmanouil, Maratou, Eirini, Ikonomidis, Ignatios, Balampanis, Konstantinos, Liatis, Stavros, Tentolouris, Nikolaos, Toulas, Panagiotis, Kousathana, Foteini, Giatzakis, Christophoros, Dimitriadis, George D., Lambadiari, Vaia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419242/
https://www.ncbi.nlm.nih.gov/pubmed/37569420
http://dx.doi.org/10.3390/ijms241512045

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419242/
https://www.ncbi.nlm.nih.gov/pubmed/37569420
http://dx.doi.org/10.3390/ijms241512045

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