Genotype-first approach reveals monogenic lipodystrophy is underdiagnosed, with health and mortality risks. [PDF]
Sharp LN +7 more
europepmc +1 more source
A Rare Instance of Concordant Charcot-Marie-Tooth Disease and Familial Partial Lipodystrophy Type 2. [PDF]
Bachir MA +4 more
europepmc +1 more source
Case Report: Twenty years of metreleptin therapy in congenital generalized lipodystrophy type 1: the longest reported follow-up to date. [PDF]
Van der Borght E +8 more
europepmc +1 more source
Lipodystrophy: an uncommon cause of insulin resistance and young-onset diabetes. [PDF]
Chaturvedi R +5 more
europepmc +1 more source
Lipodystrophies in Clinical Practice: A Case Series From a Local Health Unit in Portugal. [PDF]
Barbosa R +7 more
europepmc +1 more source
Familial partial lipodystrophy type 2 associated with a novel LMNA variant (c.604G>C; p.Glu202Gln): a Colombian family case series. [PDF]
Mendoza C, Cano R, Burgos L, Silvera CA.
europepmc +1 more source
Giant nonencapsulated pubic lipoma: a case report and literature review on differential diagnoses of atypical lipomas. [PDF]
Sabeti N +3 more
europepmc +1 more source

