Long-term Clinical Follow-up of Patients with Familial Hypomagnesemia with Secondary Hypocalcemia

• Egile Nagusiak: Elvan Bayramoğlu (Egilea), Melikşah Keskin (Egilea), Zehra Aycan (Egilea), Şenay Savaş-Erdeve (Egilea), Semra Çetinkaya (Egilea)
• Formatua: Liburua
• Argitaratua: Galenos Yayincilik, 2021-09-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Objective:Familial hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive disease caused by a mutation in the transient receptor potential melastatin 6 (TRPM6) gene and is characterized by selective magnesium malabsorption. Affected cases are usually diagnosed during infancy and...