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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 Kamrath
Published 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.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • randomized controlled trial
  • newly diagnosed
  • mental health