Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and seizures and was subsequently diagnosed with adenylosuccinate lyase deficiency. Given the rarity of this diagnosis, findings demonstrated in this case may prompt ordering physicians to broaden their approach to genetic testing in the setting of hypomyelination. Comparison is also made to more common hypomyelinating leukodystrophies. Keywords: Adenylosuccinate lyase deficiency, Hypomyelinatio
Aim: The aim of this study was to develop a high-throughput urine screening technique for adenylosuc...
Adenylosuccinate lyase deficiency is an autosomal recessive defect of purine metabolism. Succinylade...
BACKGROUND AND PURPOSE: Leukoencephalopathies of unknown origin constitute a considerable problem in...
Item does not contain fulltextAdenylosuccinate lyase (ADSL) deficiency is a rare inborn error of met...
Adenylosuccinate lyase deficiency is an autosomal-recessive disorder of the purine de novo synthesis...
Item does not contain fulltextOBJECTIVE: To describe 4 children with a novel hypomyelinating leukoen...
Contains fulltext : 88083.pdf (publisher's version ) (Closed access)Adenylosuccina...
Adenylosuccinate lyase deficiency is an autosomal-recessive disorder of the purine de novo synthesis...
Objective: To describe 4 children with a novel hypomyelinating leukoencephalopathy, defined by a dis...
BackgroundAdenylosuccinate lyase deficiency (ADSLD) is an ultrarare neurometabolic recessive disorde...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
Abstract Background Adenylosuccinate lyase (ADSL) deficiency is a defect of purine metabolism affect...
Hypomyelinating leukodystrophies constitute a subset of genetic white matter disorders characterized...
Context: In monocarboxylate transporter 8 (MCT8) gene deficiency, a syndrome combining thyroid and n...
Hypomyelinating leukodystrophies are heterogeneous genetic diseases with a wide phenotypic spectrum....
Aim: The aim of this study was to develop a high-throughput urine screening technique for adenylosuc...
Adenylosuccinate lyase deficiency is an autosomal recessive defect of purine metabolism. Succinylade...
BACKGROUND AND PURPOSE: Leukoencephalopathies of unknown origin constitute a considerable problem in...
Item does not contain fulltextAdenylosuccinate lyase (ADSL) deficiency is a rare inborn error of met...
Adenylosuccinate lyase deficiency is an autosomal-recessive disorder of the purine de novo synthesis...
Item does not contain fulltextOBJECTIVE: To describe 4 children with a novel hypomyelinating leukoen...
Contains fulltext : 88083.pdf (publisher's version ) (Closed access)Adenylosuccina...
Adenylosuccinate lyase deficiency is an autosomal-recessive disorder of the purine de novo synthesis...
Objective: To describe 4 children with a novel hypomyelinating leukoencephalopathy, defined by a dis...
BackgroundAdenylosuccinate lyase deficiency (ADSLD) is an ultrarare neurometabolic recessive disorde...
Most cases of adenylosuccinate lyase (ADSL OMIM 103050) deficiency reported to date are confined to ...
Abstract Background Adenylosuccinate lyase (ADSL) deficiency is a defect of purine metabolism affect...
Hypomyelinating leukodystrophies constitute a subset of genetic white matter disorders characterized...
Context: In monocarboxylate transporter 8 (MCT8) gene deficiency, a syndrome combining thyroid and n...
Hypomyelinating leukodystrophies are heterogeneous genetic diseases with a wide phenotypic spectrum....
Aim: The aim of this study was to develop a high-throughput urine screening technique for adenylosuc...
Adenylosuccinate lyase deficiency is an autosomal recessive defect of purine metabolism. Succinylade...
BACKGROUND AND PURPOSE: Leukoencephalopathies of unknown origin constitute a considerable problem in...