Expanding the ataxia with oculomotor apraxia type 4 phenotype

Keyphrases

• Ideomotor Apraxia 100%
• Phosphatase 60%
• Polynucleotide Kinase 60%
• Early Onset 20%
• Disease Progression 20%
• Autosomal Recessive 20%
• Obesity 20%
• Cognitive Impairment 20%
• Non-progressive 20%
• Developmental Delay 20%
• Polyneuropathy 20%
• Compound Heterozygous mutation 20%
• Intractable Seizures 20%
• Microcephaly 20%
• Chorea 20%
• Eye Movement Abnormalities 20%
• Complex Movement Disorder 20%

Biochemistry, Genetics and Molecular Biology

• Phosphatase 100%
• Kinase 100%
• Phosphotransferase 100%
• Polynucleotide 100%
• Eye Movement 33%
• Autosomal Recessive Disorder 33%

Neuroscience

• Ataxia 100%
• Apraxia 100%
• Phosphatase 60%
• Polynucleotide 5' Hydroxyl Kinase 60%
• Eye Movement 20%
• Cognitive Disorders 20%
• Stereotypic Movement Disorder 20%
• Polyneuropathy 20%
• Autosomal Recessive Disorder 20%
• Chorea 20%
• Microcephaly 20%