Congenital generalized lipodystrophy type 4 due to a novel PTRF/CAVIN1 pathogenic variant in a child: effects of metreleptin substitution.
Süleyman Cem AdiyamanJulia V SchnurbeinJan De LaffolieAndreas HahnReiner SiebertMartin WabitschClemens KamrathPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2022)
Although CGL4 is rare, due to its life-threatening comorbidities and the opportunity for an early intervention, it is important that the clinicians should recognise these patients.