Patients' perspective on the medical pathway from first symptoms to diagnosis in genetic lipodystrophy.
Helena MosbahCamille VatierBéatrice AndrissInès BelalemBrigitte DelemerSonja JanmaatIsabelle JéruLauriane Le CollenDominique MaiterEstelle NobécourtMarie-Christine Vantyghemnull nullCorinne VigourouxAgnes DumasPublished in: European journal of endocrinology (2023)
Diagnostic pathway in patients with genetic lipodystrophy is rendered difficult by the multisystemic features of the disease and the lack of knowledge of non-specialized physicians. Training physicians to systematically include adipose tissue examination in routine clinical evaluation should improve diagnosis and management of lipodystrophy and lipodystrophy-associated comorbidities.
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