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...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:JCRPE
المؤلفون الرئيسيون: Elvan Bayramoğlu, Melikşah Keskin, Zehra Aycan, Şenay Savaş-Erdeve, Semra Çetinkaya
التنسيق: مقال
اللغة:الإنجليزية
منشور في: Pediatric Endocrinology and Diabetes Society 2021-09-01
الموضوعات:
hypomagnesemia
hypocalsemia
trpm6 mutation
الوصول للمادة أونلاين: http://www.jcrpe.org/archives/archive-detail/article-preview/long-term-clinical-follow-up-of-patients-with-fami/44077

الانترنت

http://www.jcrpe.org/archives/archive-detail/article-preview/long-term-clinical-follow-up-of-patients-with-fami/44077

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