Biotin-thiamine responsive basal ganglia disease: a retrospective review of the clinical, radiological and molecular findings of cases in Kuwait with novel variants

BACKGROUND: Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare autosomal recessive neurometabolic disorder that is caused by biallelic pathogenic SLC19A3 variants and is characterized by subacute encephalopathy associated with confusion, convulsions, dysphagia, dysarthria, or other n...

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Detalles Bibliográficos
Autores principales: Aburezq, Maryam, Alahmad, Ahmad, Alsafi, Rasha, Al-Tawari, Asma, Ramadan, Dina, Shafik, Magdy, Abdelaty, Omar, Makhseed, Nawal, Elshafie, Reem, Ayed, Mariam, Hayat, Abrar, Dashti, Fatima, Marafi, Dana, Albash, Buthaina, Bastaki, Laila, Alsharhan, Hind
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478457/
https://www.ncbi.nlm.nih.gov/pubmed/37670342
http://dx.doi.org/10.1186/s13023-023-02888-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10478457/
https://www.ncbi.nlm.nih.gov/pubmed/37670342
http://dx.doi.org/10.1186/s13023-023-02888-y

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