Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation
Hypomagnesemia is a rare cause of seizures in childhood but should be kept in mind in recurrent and intractable seizures and hypocalcemia in communities where consanguineous marriages are common. Familial hypomagnesemia with secondary hypocalcemia is a rare genetic cause of hypomagnesemia, due to va...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Pediatric Endocrinology and Diabetes Society
2021-03-01
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| Seri Bilgileri: | JCRPE |
| Konular: | |
| Online Erişim: |
http://www.jcrpe.org/archives/archive-detail/article-preview/treatment-difficulties-in-hypomagnesemia-secondary/37305
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