Phosphatdiabetes: Understanding the X-Chromosomal Hypophosphatemia

Phosphatdiabetes, also known as X-chromosomal hypophosphatemia, is a rare, inherited multi-organ disease primarily affecting the skeletal system and teeth. The pathophysiology of XLH is complex, leading to a broad spectrum of different organ manifestations and symptoms. As a result, various medical specialists, therapists, and social professionals are involved in the care of these patients.

The monograph provides a comprehensive overview of the history, pathogenesis, diagnosis, and therapeutic options for XLH. It offers insights for the numerous professionals involved in patient care, contributing significantly to the recognition of this rare disease and providing valuable information for multidisciplinary care teams on how to best support affected patients and their families.

Product Details:

ASIN: B0BMQ6S2R1

Publisher: UNI-MED Verlag AG; 1st edition (November 16, 2022)

Publication Date: November 16, 2022

Language: German