A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant.
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| Title: | A Rare Case of Neonatal Hypomagnesemia with Secondary Hypocalcemia Caused by a Novel Homozygous TRPM6 Gene Variant. |
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| Authors: | Uddin MS; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alradhi AY; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alqathani FMN; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alessa OS; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Alshammari ANM; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia., Tripathy R; Department of Human Genetics, Bioscientia Institute for Medical Diagnostics GmbH, Ingelheim, Germany., Alomari MA; Department of Pediatrics, Ministry of National Guard Health Affairs, Dammam, Saudi Arabia. |
| Source: | The American journal of case reports [Am J Case Rep] 2024 Mar 26; Vol. 25, pp. e942498. Date of Electronic Publication: 2024 Mar 26. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 101489566 Publication Model: Electronic Cited Medium: Internet ISSN: 1941-5923 (Electronic) Linking ISSN: 19415923 NLM ISO Abbreviation: Am J Case Rep Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1941-5923 |
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| DOI: | 10.12659/AJCR.942498 |
