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

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...

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Detalles Bibliográficos
Autores principales: Bayramoğlu, Elvan, Keskin, Melikşah, Aycan, Zehra, Savaş-Erdeve, Şenay, Çetinkaya, Semra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388043/
https://www.ncbi.nlm.nih.gov/pubmed/33565749
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2020.0192

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388043/
https://www.ncbi.nlm.nih.gov/pubmed/33565749
http://dx.doi.org/10.4274/jcrpe.galenos.2021.2020.0192

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