New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis
Magali Colombat, Jean‐Claude Aldigier, Pierre-Raphaël Rothschild, Vincent Javaugue, Éstelle Desport, T. Frouget, Jean‐Michel Goujon, Nathalie Rioux-Leclercq, Nathalie Quellard, Jean Philippe Rerolle, François Paraf, Caroline Beugnet, A. Tiple, Antoine Dürrbach, Didier Samuel, Antoine P. Brézin, Frank Bridoux, Sophie Valleix
Topics & Concepts
AmyloidosisAL amyloidosisPathologyMedicineAmyloid (mycology)TransplantationPenetranceBiologyInternal medicinePhenotypeImmunologyGeneticsGeneImmunoglobulin light chainAntibodyAmyloidosis: Diagnosis, Treatment, OutcomesDermatological and Skeletal DisordersRenal Diseases and Glomerulopathies