LESCH – NYHAN SYNDROME (LNS) - THE REVIEW

Lesch-Nyhan syndrome (LNS) is a rare X-linked disorder caused by mutations in the HPRT1 gene, which encodes an important enzyme in the purine salvage pathway. Symptoms of LNS include dystonia, gout, intellectual disability, and self-harm. Although the disease was described in 1964, it remains unclear how abnormalities in hypoxanthine and guanine recycling can lead to such significant neurological deficits. Several studies have proposed different hypotheses regarding the etiology of the disease and various treatment options have been proposed, but none have led to a satisfactory explanation of the pathophysiology of the disease. New technologies such as sequencing, optogenetics, genome editing, and induced pluripotent stem cells may provide a unique opportunity to map the precise sequential pathways from genotype to disease phenotype.

Authors

Institutions

Publication Details

Journal
International Journal of Innovative Technologies in Social Science
Published
2025-09-30
DOI
https://doi.org/10.31435/ijitss.3(47).2025.3862
Primary Topic
Biochemical and Molecular Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

LESCH – NYHAN SYNDROME (LNS) - THE REVIEW

Daria Madycka, Małgorzata Słaboń, Karol Stępniak, Joanna Wrona et al.
International Journal of Innovative Technologies in Social Science
Biochemical and Molecular Research
article

LESCH – NYHAN SYNDROME (LNS) - THE REVIEW

Daria Madycka, Małgorzata Słaboń, Karol Stępniak, Joanna Wrona, Kinga Wnuczek, Wiktor Telega, Aleksandra Kaźmierczyk, Jędrzej Kęsik, Weronika Skrzypek
article en

Abstract

Lesch-Nyhan syndrome (LNS) is a rare X-linked disorder caused by mutations in the HPRT1 gene, which encodes an important enzyme in the purine salvage pathway. Symptoms of LNS include dystonia, gout, intellectual disability, and self-harm. Although the disease was described in 1964, it remains unclear how abnormalities in hypoxanthine and guanine recycling can lead to such significant neurological deficits. Several studies have proposed different hypotheses regarding the etiology of the disease and various treatment options have been proposed, but none have led to a satisfactory explanation of the pathophysiology of the disease. New technologies such as sequencing, optogenetics, genome editing, and induced pluripotent stem cells may provide a unique opportunity to map the precise sequential pathways from genotype to disease phenotype.

International Journal of Innovative Technologies in Social ScienceVol. 5(3(47))
1 Military Clinical Hospital with Outpatient Clinic (PL)
Openalex Percentile: Top 75%
Biochemical and Molecular Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.