Encephalopathies with neostriatal involvement constitute a heterogeneous group of acquired and genetically inherited conditions that include Bilateral Striatal Necrosis (BSN) and other Striatal Lesions (SL) (Tonduti et al). We describe two new patients suffering from BSN due to biallelic SLC19A3 mutations. In the first patient vitamin supplementation was started early on, resulting in the remission of the clinical picture, and an almost complete normalization of the neuroradiological findings. In the second one treatment was started late, compliance was irregular and the resulting clinical outcome was poor. The clinical outcome of our two patients confirms and further stresses the importance of the early administration of vitamin supplement...
We are grateful for the opportunity to respond to the correspond-ence from Haack et al. (2014) and t...
Background TTC19 deficiency is a progressive neurodegenerative disease associated with isolated mit...
Background: Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare treatable autosomal r...
The research articles ‘Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile,...
Abstract Background SLC19A3 (solute carrier family 19, member 3) is a thiamin transporter with 12 tr...
Aim: To present seven new genetically confirmed cases of biotin-thiamin-responsive basal ganglia dis...
WOS: 000455065100029PubMed ID: 30054086Background: Biotin-thiamine responsive basal ganglia disease ...
Biotin-thiamine responsive basal ganglia disease (BTRBGD) is an autosomal recessive neurometabolic d...
Thiamine metabolism dysfunction syndrome 2 (THMD2) is a rare metabolic disorder caused by SLC19A3 mu...
Abstract Background Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare autosomal rec...
BACKGROUND:Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable d...
Background: Bilateral striatal necrosis (BSN) is characterized by symmetrical degeneration, predomin...
Primary and secondary conditions leading to thiamine deficiency have overlapping features in childre...
To accomplish a diagnosis in patients with a rare unclassified disorder is difficult. In this study,...
We report about a patient with infantile-onset neurodegenerative disease associated with isolated mi...
We are grateful for the opportunity to respond to the correspond-ence from Haack et al. (2014) and t...
Background TTC19 deficiency is a progressive neurodegenerative disease associated with isolated mit...
Background: Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare treatable autosomal r...
The research articles ‘Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile,...
Abstract Background SLC19A3 (solute carrier family 19, member 3) is a thiamin transporter with 12 tr...
Aim: To present seven new genetically confirmed cases of biotin-thiamin-responsive basal ganglia dis...
WOS: 000455065100029PubMed ID: 30054086Background: Biotin-thiamine responsive basal ganglia disease ...
Biotin-thiamine responsive basal ganglia disease (BTRBGD) is an autosomal recessive neurometabolic d...
Thiamine metabolism dysfunction syndrome 2 (THMD2) is a rare metabolic disorder caused by SLC19A3 mu...
Abstract Background Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare autosomal rec...
BACKGROUND:Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable d...
Background: Bilateral striatal necrosis (BSN) is characterized by symmetrical degeneration, predomin...
Primary and secondary conditions leading to thiamine deficiency have overlapping features in childre...
To accomplish a diagnosis in patients with a rare unclassified disorder is difficult. In this study,...
We report about a patient with infantile-onset neurodegenerative disease associated with isolated mi...
We are grateful for the opportunity to respond to the correspond-ence from Haack et al. (2014) and t...
Background TTC19 deficiency is a progressive neurodegenerative disease associated with isolated mit...
Background: Biotin-thiamine-responsive basal ganglia disease (BTBGD) is a rare treatable autosomal r...