Arginase 1 Deficiency in Patients Initially Diagnosed with Hereditary Spastic Paraplegia

Keyphrases

• Hereditary Spastic Paraplegia 100%
• Arginase Deficiency 100%
• Lower Limb Spasticity 30%
• Arginine 20%
• Urea Cycle Disorders 20%
• Disease Progression 10%
• Genetic Causes 10%
• Pathologic 10%
• Differential Diagnosis 10%
• Hispanic 10%
• Seizure 10%
• Sudden Onset 10%
• Autosomal Recessive 10%
• Retrospective Analysis 10%
• Medical History 10%
• Developmental Delay 10%
• Arginase-1 (Arg-1) 10%
• Loss Function 10%
• Hispanic Women 10%
• Accurate Diagnosis 10%
• Childhood-onset 10%
• Treatment Delay 10%
• Diagnostic Delay 10%
• Deficiency Diagnosis 10%
• Clinical Similarity 10%
• Disease Awareness 10%
• Gait Abnormalities 10%
• Gene Panel 10%
• Onset Manifestations 10%
• Progressive Spasticity 10%

Medicine and Dentistry

• DeJerine-Sottas Disease 100%
• Arginase 1 100%
• Spasticity 40%
• Lower Limb 30%
• Arginine 20%
• Urea Cycle Disorder 20%
• Disease Exacerbation 10%
• Differential Diagnosis 10%
• Awareness 10%
• Autosomal Recessive Inheritance 10%
• Gait 10%
• Epileptic Seizure 10%
• Developmental Delay 10%
• Therapy Delay 10%
• Diagnostic Delay 10%
• Diseases 10%
• Genetics 10%
• Medical History 10%

Biochemistry, Genetics and Molecular Biology

• Arginase 100%
• Deficiency 100%
• Urea Cycle Disorder 20%
• Blood Plasma 20%
• Arginine 20%
• Genetics 10%
• Autosomal Recessive Inheritance 10%
• Awareness 10%
• Gait 10%
• ARG1 10%