Global Variome shared LOVD

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Phenotype #0000229898 Individual ID 00302816 Associated disease NBIA Phenotype details walk-2y; febrile convulsion at infant; no speech; cognitive dysfunction during childhood; developmental delay, intellectual disability; wheelchair bound; cognitive dysfunction; 32y-Parkinsonism, rigidity, no tremor; postural abnormality; no dystonia; increasing deep tendon reflex; no appearances of pathologic reflex; progressive dementia during adulthood; no psychiatric symptoms; epileptic seizure; excellent Levodopa responsive; no Levodopa-induced dyskinesia; no RETT-like features; no sleep problems; no ocular defects; EEG normal; MRI brain T2 hypointense substantia nigra and globus pallidus (high iron), T1 hyperintense ‘halo’ in midbrain, no eye-of-the-tiger sign, no white matter involvement, diffuse cerebral atrophy (rt < lt), no cerebellar atrophy Diagnosis/Initial neurodegeneration with brain iron accumulation Inheritance Isolated (sporadic) Diagnosis/Definite NBIA5 Age/Examination 33y (33 years) Age/Onset - Phenotype/Onset cognitive dysfunction Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-06-01 13:42:38 +02:00 (CEST) Date last edited N/A

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