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The Importance of Networking in Pseudohypoparathyroidism: EuroPHP Network and Patient Support Associations
Agnès Linglart1, Giovanna Mantovani2, Intza Garin3
1APHP, Reference center for rare disorders of the mineral metabolism and Plateforme d'expertise Paris Sud Maladies Rares, Le Kremlin Bicêtre, France, INSERM U1169, Hôpital Bicêtre, Le Kremlin Bicêtre, et Université Paris-Saclay, France.
Abstract:
Pseudohypoparathyroidism is a rare endocrine disorder with an estimated prevalence of 1/100,000. It is characterized by hypocalcemia and hyperphosphatemia in the absence of vitamin D deficiency or impaired renal function. Research studies during the last 20 years have led to the identification of the molecular underlying cause of the disease, the characterization of the clinical and biochemical characteristics and the observation of an overlap between genetic and clinical manifestations. The creation of networks both for specialists (including endocrinologists, pediatricians, dermatologists, geneticists, molecular biologists…) and patients support groups brings up the opportunity of research advance, synergism and common objectives for families and investigators, improving the quality of information about the disease and its outcome, that, at the end, will improve both the knowledge and life of the patients and their families.
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