Neonatal Hypocalcemic Seizures in Offspring of a Mother With Familial Hypocalciuric Hypercalcemia Type 1 (FHH1)

CONTEXT: Familial hypocalciuric hypercalcemia type 1 (FHH1) is caused by loss-of-function mutations of the calcium-sensing receptor (CaSR) and is considered a benign condition associated with mild-to-moderate hypercalcemia. However, the children of parents with FHH1 can develop a variety of disorder...

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Detalles Bibliográficos
Publicado en:J Clin Endocrinol Metab
Autores principales: Dharmaraj, Poonam, Gorvin, Caroline M, Soni, Astha, Nelhans, Nick D, Olesen, Mie K, Boon, Hannah, Cranston, Treena, Thakker, Rajesh V, Hannan, Fadil M
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2020
Materias:
Clinical Research Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7096312/
https://ncbi.nlm.nih.gov/pubmed/32150253
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/clinem/dgaa111
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