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Hypophosphatemia due to chronically increased renalphosphate clearance leads to variable bone diseasessuch as rickets and osteomalacia. The most commoninherited form of hypophosphatemia is X-linkedhypophosphatemic rickets. Other inherited forms ofthe disease are autosomal dominant and recessivehypophosphatemic rickets.This work should give a summary of the latestfindings in this hypophosphatemic disease anddiscusses reasons which lead to the illness. A lot ofpatients and also the two brothers who were discussedin this case report have clear hypophosphatemicsymptoms but no genetic reasons were…mehr

Produktbeschreibung
Hypophosphatemia due to chronically increased renalphosphate clearance leads to variable bone diseasessuch as rickets and osteomalacia. The most commoninherited form of hypophosphatemia is X-linkedhypophosphatemic rickets. Other inherited forms ofthe disease are autosomal dominant and recessivehypophosphatemic rickets.This work should give a summary of the latestfindings in this hypophosphatemic disease anddiscusses reasons which lead to the illness. A lot ofpatients and also the two brothers who were discussedin this case report have clear hypophosphatemicsymptoms but no genetic reasons were found. Thisdisease gives also new cognitions about phosphatehomeostasis, althoug a lot of questions still remain.
Autorenporträt
Karolina Horner wurde 1980 in Wien geboren. 2007 schloß sie ihrMedizinstudium mit der vorliegenden Dissertation ab. Anschließendarbeitete sie als wissenschaftliche Mitarbeiterin auf derUniversitätsklinik für Kinderheilkunde in Wien und absolviertderzeit einen Teil ihrer Ausbildung bei einem niedergelassenenKinderarzt.