hrp0086p2-p173 | Bone & Mineral Metabolism P2 | ESPE2016
, Cartigny Maryse
, Lefevre Christine
, Weill Jacques
Background: Bartter syndrome represents a rare severe condition, autosomal recessive, corresponding to several genes, characterized by an illness of the renal ascending branch of the handle of Henle. Only 15 cases of BSHPT have been communicated, either in publications or orally, but none presented such severe bone manifestation as ours.Objective and hypotheses: To present bone features of two patients suffering from severe BHSPT, so as the therapeutic a...