Full-Mouth Rehabilitation of a 15-Year-Old Girl Affected by a Rare Hypoparathyroidism (Glial Cell Missing Homolog 2 Mutation): A 3-Year Follow-Up

• المؤلفون الرئيسيون: Yohann Flottes (مؤلف), Eléonore Valleron (مؤلف), Bruno Gogly (مؤلف), Claudine Wulfman (مؤلف), Elisabeth Dursun (مؤلف)
• التنسيق: كتاب
• منشور في: MDPI AG, 2024-05-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Objective: Familial isolated hypoparathyroidism is a rare genetic disorder due to no or low production of the parathyroid hormone, disturbing calcium and phosphate regulation. The resulting hypocalcemia may lead to dental abnormalities, such as enamel hypoplasia. The aim of this paper was to describ...