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Maladies métaboliques et nutritionnelles
Maladies métaboliques
Erreurs innées du métabolisme
Maladies lysosomiales
Maladies neurologiques de surcharge lysosomiale
Maladies neurologiques de surcharge lysosomiale : Questions médicales fréquentes
Diagnostic
5
Maladies lysosomales
Diagnostic médical
Biopsie
Imagerie par résonance magnétique
Symptômes neurologiques
Maladies lysosomales
Antécédents familiaux
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Maladies lysosomales
Symptômes
5
Symptômes neurologiques
Troubles du développement
Maladies lysosomales
Symptômes neurologiques
Troubles psychologiques
Maladies neurologiques
Âge d'apparition
Maladies neurologiques
Symptômes neurologiques
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Prévention
5
Prévention
Dépistage génétique
Conseil génétique
Maladies héréditaires
Vaccination
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Traitements
5
Thérapie enzymatique
Traitement médical
Thérapie génique
Maladies lysosomales
Médicaments
Symptômes neurologiques
Essais cliniques
Traitements expérimentaux
Physiothérapie
Réhabilitation
Complications
5
Complications
Maladies neurologiques
Gestion des complications
Traitement précoce
Qualité de vie
Complications
Mortalité
Maladies lysosomales
Complications
Gestion à long terme
Facteurs de risque
5
Facteurs de risque
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Âge parental
Facteurs de risque
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Maladies héréditaires
Facteurs environnementaux
Maladies génétiques
Hérédité
Maladies lysosomales
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"@type": "Question",
"name": "Comment diagnostique-t-on ces maladies ?",
"position": 1,
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"text": "Le diagnostic repose sur des tests génétiques, des analyses enzymatiques et des imageries cérébrales."
}
},
{
"@type": "Question",
"name": "Quels tests sont utilisés pour le diagnostic ?",
"position": 2,
"acceptedAnswer": {
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"text": "Des tests sanguins, des biopsies et des examens d'imagerie comme l'IRM sont courants."
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"@type": "Question",
"name": "Les symptômes aident-ils au diagnostic ?",
"position": 3,
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"@type": "Question",
"name": "Les antécédents familiaux sont-ils importants ?",
"position": 4,
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"@type": "Question",
"name": "Peut-on diagnostiquer in utero ?",
"position": 5,
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"text": "Oui, des tests génétiques peuvent être réalisés pendant la grossesse pour certaines maladies."
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"@type": "Question",
"name": "Quels sont les symptômes courants ?",
"position": 6,
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"text": "Les symptômes incluent des troubles moteurs, des convulsions, et des retards de développement."
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"@type": "Question",
"name": "Les symptômes varient-ils selon la maladie ?",
"position": 7,
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"text": "Oui, chaque maladie lysosomale présente un ensemble unique de symptômes neurologiques."
}
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"@type": "Question",
"name": "Y a-t-il des symptômes psychologiques associés ?",
"position": 8,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des troubles de l'humeur et des problèmes cognitifs peuvent également se manifester."
}
},
{
"@type": "Question",
"name": "Les symptômes apparaissent-ils à un âge spécifique ?",
"position": 9,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les symptômes peuvent apparaître à différents âges, souvent dans l'enfance ou l'adolescence."
}
},
{
"@type": "Question",
"name": "Les symptômes sont-ils réversibles ?",
"position": 10,
"acceptedAnswer": {
"@type": "Answer",
"text": "Non, les symptômes sont généralement progressifs et irréversibles sans traitement approprié."
}
},
{
"@type": "Question",
"name": "Peut-on prévenir ces maladies ?",
"position": 11,
"acceptedAnswer": {
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"text": "La prévention est limitée, mais le dépistage génétique peut aider à identifier les porteurs."
}
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"@type": "Question",
"name": "Le conseil génétique est-il recommandé ?",
"position": 12,
"acceptedAnswer": {
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"text": "Oui, le conseil génétique est conseillé pour les familles à risque de maladies lysosomales."
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"@type": "Question",
"name": "Les vaccinations sont-elles importantes ?",
"position": 13,
"acceptedAnswer": {
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"text": "Les vaccinations ne préviennent pas les maladies lysosomales, mais sont essentielles pour la santé générale."
}
},
{
"@type": "Question",
"name": "Y a-t-il des mesures préventives spécifiques ?",
"position": 14,
"acceptedAnswer": {
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"text": "Aucune mesure préventive spécifique n'existe, mais un suivi médical régulier est conseillé."
}
},
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"@type": "Question",
"name": "Les tests de dépistage sont-ils utiles ?",
"position": 15,
"acceptedAnswer": {
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"text": "Oui, les tests de dépistage peuvent identifier les porteurs et aider à la planification familiale."
}
},
{
"@type": "Question",
"name": "Quels traitements sont disponibles ?",
"position": 16,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les traitements incluent la thérapie enzymatique de remplacement et la gestion des symptômes."
}
},
{
"@type": "Question",
"name": "La thérapie génique est-elle une option ?",
"position": 17,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, la thérapie génique est en cours d'étude pour certaines maladies lysosomales."
}
},
{
"@type": "Question",
"name": "Les médicaments peuvent-ils soulager les symptômes ?",
"position": 18,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des médicaments peuvent aider à gérer les symptômes neurologiques et comportementaux."
}
},
{
"@type": "Question",
"name": "Y a-t-il des traitements expérimentaux ?",
"position": 19,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, des essais cliniques explorent de nouvelles approches thérapeutiques pour ces maladies."
}
},
{
"@type": "Question",
"name": "La physiothérapie est-elle bénéfique ?",
"position": 20,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, la physiothérapie peut aider à améliorer la mobilité et la qualité de vie des patients."
}
},
{
"@type": "Question",
"name": "Quelles complications peuvent survenir ?",
"position": 21,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les complications incluent des troubles neurologiques graves, des problèmes cardiaques et respiratoires."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles évitables ?",
"position": 22,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines complications peuvent être gérées, mais beaucoup sont inévitables sans traitement précoce."
}
},
{
"@type": "Question",
"name": "Les complications affectent-elles la qualité de vie ?",
"position": 23,
"acceptedAnswer": {
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"text": "Oui, les complications neurologiques peuvent gravement affecter la qualité de vie des patients."
}
},
{
"@type": "Question",
"name": "Y a-t-il des risques de décès ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines maladies lysosomales peuvent entraîner un risque accru de mortalité précoce."
}
},
{
"@type": "Question",
"name": "Les complications sont-elles réversibles ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Non, la plupart des complications sont irréversibles et nécessitent une gestion à long terme."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque génétiques ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les antécédents familiaux de maladies lysosomales augmentent le risque de transmission génétique."
}
},
{
"@type": "Question",
"name": "L'âge des parents influence-t-il le risque ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, l'âge avancé des parents peut augmenter le risque de mutations génétiques."
}
},
{
"@type": "Question",
"name": "Les origines ethniques jouent-elles un rôle ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines populations ont un risque plus élevé de maladies lysosomales en raison de la consanguinité."
}
},
{
"@type": "Question",
"name": "Y a-t-il des facteurs environnementaux ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Actuellement, les facteurs environnementaux ne sont pas clairement établis comme des risques."
}
},
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"@type": "Question",
"name": "Les maladies lysosomales sont-elles héréditaires ?",
"position": 30,
"acceptedAnswer": {
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"text": "Oui, la plupart des maladies lysosomales sont héréditaires et se transmettent selon des modèles génétiques."
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Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 21/01/2026
Contenu vérifié selon les dernières recommandations médicales
4 publications dans cette catégorie
Affiliations :
Department of Veterinary Medicine and Animal Productions, University of Naples Federico II, Via Federico Delpino 1, 80137 Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
4 publications dans cette catégorie
Affiliations :
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via Sergio Pansini 5, 80131 Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
3 publications dans cette catégorie
Affiliations :
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via Sergio Pansini 5, 80131 Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
3 publications dans cette catégorie
Affiliations :
Department of Molecular Biology, Faculty of Biology, University of Gdansk, Gdansk, Poland.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
3 publications dans cette catégorie
Affiliations :
Molecular Neurogenetics Section, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: sidranse@mail.nih.gov.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Cell and Developmental Biology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Pharmacology, University of Oxford, Oxford, UK. frances.platt@pharm.ox.ac.uk.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Office of the Clinical Director and Medical Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
1 University of Florida, Departments of Pediatrics, Division of Genetics and Metabolism, Neuroscience and Molecular Genetics & Microbiology, Gainesville, FL, USA.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via Sergio Pansini 5, 80131 Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Molecular Medicine and Medical Biotechnologies, University of Naples Federico II, Via Sergio Pansini 5, 80131 Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.
Department of Translational Medical Sciences, Section of Pediatrics, Federico II University, Naples, Italy.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Institute for the Study of Inborn Errors of Metabolism, Faculty of Science, Pontificia Universidad Javeriana, Cra. 7 No. 43-82 Building 54, Room 305A, Bogotá D.C, 110231, Colombia.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Institute for the Study of Inborn Errors of Metabolism, Faculty of Science, Pontificia Universidad Javeriana, Cra. 7 No. 43-82 Building 54, Room 305A, Bogotá D.C, 110231, Colombia. cjalmeciga@javeriana.edu.co.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Medical Genetics Service, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Genetics, Federal University of Rio Grande do Sul, Porto Alegre, Brazil.
Gene Therapy Center, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, USA; Department of Molecular Biology, Faculty of Biology, University of Gdansk, Gdansk, Poland; Faculty of Arts and Sciences, University of Delaware, Newark, DE, USA; Department of Pediatrics, Graduate School of Medicine, Gifu University, Gifu, Japan; Department of Pediatrics, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address: shunji.tomatsu@nemours.com.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Pediatric Metabolism, Ankara Bilkent City Hospital, Ankara, Turkey.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Cell Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan; Department of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan. Electronic address: kidojun@kuh.kumamoto-u.ac.jp.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
2 publications dans cette catégorie
Affiliations :
Department of Pediatrics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Publications dans "Maladies neurologiques de surcharge lysosomiale" :
Lysosomal storage diseases are a group of rare hereditary metabolic diseases. Due to a deficiency of lysosomal enzymes, complex substrates accumulate in the lysosomes of various organs. Depending on t...
Lysosomal storage disorders (LSD) are a heterogenous group of inborn errors of metabolism due to lysosomal malfunction. LSDs affect 1 in 5000 live births, albeit every LSD itself has a low incidence. ...
Lysosomal storage disorders (LSD) are a group of inherited inborn metabolism errors that are characterized by a deficiency in the lysosomal enzyme. In patients with suspected lipid storage disorders, ...
Clinical findings of hepatomegaly and splenomegaly, the abnormal enlargement of the liver and spleen, respectively, should prompt a broad differential diagnosis that includes metabolic, congestive, ne...
Lysosomal storage diseases (LSDs) are caused by monogenic mutations in genes encoding for proteins related to the lysosomal function. Lysosome plays critical roles in molecule degradation and cell sig...
Genetic substrate reduction therapy (gSRT), which involves the use of nucleic acids to downregulate the genes involved in the biosynthesis of storage substances, has been investigated in the treatment...
To analyze the application of gSRT to the treatment of LSDs, identifying the silencing tools and delivery systems used, and the main challenges for its development and clinical translation, highlighti...
A systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) reporting guidelines was performed. PubMed, Scopus, and Web of Science databases were used...
Fabry, Gaucher, and Pompe diseases and mucopolysaccharidoses I and III are the only LSDs for which gSRT has been studied, siRNA and lipid nanoparticles being the silencing strategy and the delivery sy...
Nucleic acid therapies are expanding the clinical tools and therapies currently available for LSDs. Recent advances in CRISPR/Cas9 technology and the growing impact of nanotechnology are expected to b...
Dysregulated lipid metabolism contributes to neurodegenerative pathologies and neurological decline in lysosomal storage disorders as well as more common neurodegenerative diseases. Niemann-Pick type ...
Historically, the clinical manifestations of lysosomal storage diseases offered an early glimpse into the essential digestive functions of the lysosome. However, it was only recently that the more sub...
Thesaurismosis or storage diseases are rare genetic disorders due to an abnormal accumulation of an organic compound or its metabolite within cells. These conditions are either secondary to a defect i...
Lysosomal storage diseases (LSDs) are a group of metabolic disorders resulting from a deficiency in one of the lysosomal hydrolases. Most LSDs are inherited in an autosomal or X-linked recessive manne...