17q12 Deletion Syndrome with Convulsions and Family History of Increased Intracranial Pressure Syndrome

17q12 Deletion Syndrome


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https://doi.org/10.5281/zenodo.13956038

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References

Mitchel MW, Moreno-De-Luca D, Myers SM, Levy RV, Turner S, Ledbetter DH, Martin CL. 17q12 Recurrent Deletion Syndrome. 2016 Dec 8 [updated 2020 Oct 15]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.

Bockenhauer D, Jaureguiberry G. HNF1B-associated clinical phenotypes: the kidney and beyond. Pediatr Nephrol. 2016 May;31(5):707-14. doi: 10.1007/s00467-015-3142-2. Epub 2015 Jul 8.

q12 deletion syndrome. Accessed at: 17.10.2024 https://medlineplus.gov/genetics/condition/17q12-deletion-syndrome/

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2024-10-20

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Demir, M. E., Gök, F., Terzi, P., & Sezer, S. (2024). 17q12 Deletion Syndrome with Convulsions and Family History of Increased Intracranial Pressure Syndrome: 17q12 Deletion Syndrome . Journal of European Internal Medicine Professionals, 2(4), 139–140. https://doi.org/10.5281/zenodo.13956038

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Vol. 2 No. 4 (2024): J Eur Int Med Prof

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Letter to Editor

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Copyright (c) 2024 Mehmet Emin Demir, Faysal Gök, Pelin Terzi, Siren Sezer

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This work is licensed under a Creative Commons Attribution 4.0 International License.