Varaico: Literature-Extracted Genetic Variants

Gene:SGPL1
Variant:p.G360V
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SGPL1

NM_003901.4:p.G360V

Associated Papers

Factors influencing survival in sphingosine phosphate lyase insufficiency syndrome: a retrospective cross-sectional natural history study of 76 patients.

Keller N et al.

Orphanet Journal of Rare Diseases, 2024

Prevalence estimate of sphingosine phosphate lyase insufficiency syndrome in worldwide and select populations.

Sedillo JC et al.

Genetics in Medicine Open, 2024

Sphingosine phosphate lyase insufficiency syndrome: a systematic review.

Pournasiri Z et al.

World Journal of Pediatrics : Wjp, 2023

A rare cause of nephrotic syndrome-sphingosine-1-phosphate lyase (SGPL1) deficiency: 6 cases and a review of the literature.

Tastemel Ozturk T et al.

Pediatric Nephrology (berlin, Germany), 2023

Steroid-resistant nephrotic syndrome associated with certain SGPL1 variants in a family: Case report and literature review.

Yang S et al.

Frontiers in Pediatrics, 2023

Congenital adrenal calcifications as the first clinical indication of sphingosine lyase insufficiency syndrome: A case report and review of the literature.

Ron HA et al.

American Journal of Medical Genetics. Part A, 2022

A retrospective analysis of endocrine disease in sphingosine-1-phosphate lyase insufficiency: case series and literature review.

Maharaj A et al.

Endocrine Connections, 2022

Genotype/Phenotype Interactions and First Steps Toward Targeted Therapy for Sphingosine Phosphate Lyase Insufficiency Syndrome.

Saba JD et al.

Cell Biochemistry and Biophysics, 2021

MRI Spectrum of Brain Involvement in Sphingosine-1-Phosphate Lyase Insufficiency Syndrome.

Martin KW et al.

Ajnr. American Journal of Neuroradiology, 2020

Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation.

Zhao P et al.

Journal of Inherited Metabolic Disease, 2020

Persistent hypoglycemic attacks during hemodialysis sessions in an infant with congenital nephrotic syndrome: Answers.

Saygili S et al.

Pediatric Nephrology (berlin, Germany), 2019

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."