Right now, families affected by SYNGAP1 are doing everything they can to manage daily seizures, behavioral struggles, and unanswered questions. At Johns Hopkins, scientists believe they are within five years of a treatment. A therapy that targets the source of the disorder, not just the symptoms. But NIH funding cuts are threatening to stop that progress. Learn more about what’s at stake: https://hub.jhu.edu/2025/05/14/rare-genetic-disorders-syngap1/ #ResearchSavesLives | Johns Hopkins Universit
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FacebookJohns Hopkins University
Right now, families affected by SYNGAP1 are doing everything they can to manage daily seizures, behavioral struggles, and unanswered questions. At Johns Hopkins,
Johns Hopkins University. . Right now, families affected by SYNGAP1 are doing everything they can to manage daily seizures, behavioral struggles, and unanswered questions. At Johns Hopkins, scientists believe they are within five years of a treatment. A therapy that targets the source of the disorder, not just the symptoms. But NIH funding cuts ...
2K views11 months ago
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Syndrome SYNGAP1 : quand l’accès à l’école pour les enfants en situation de handicap est difficile
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konbini.comApr 3, 2024
Lévi, 7 ans, est atteint du syndrome SYNGAP1. Comme lui, un enfant handicapé sur quatre ne peut pas aller à l’école. Sa mère, Fiona, raconte les difficultés qu’elle rencontre au quotidien pour le scolariser et espère un changement du système éducatif. | Konbini news
Lévi, 7 ans, est atteint du syndrome SYNGAP1. Comme lui, un enfant handicapé sur quatre ne peut pas aller à l’école. Sa mère, Fiona, raconte les difficultés qu’elle rencontre au quotidien pour le scolariser et espère un changement du système éducatif. | Konbini news
FacebookSep 8, 2023
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