CEREBELLAR DISORDERS CHILDHOOD

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BASAL GANGLIA DISORDERS

PLAN (PLA2G6)

HYPOINTENSITY (SWI/ GRE)

GLOBUS PALLIDUS

PUTAMEN/ CAUDATE

SUBSTANTIA NIGRA

ATROPHY

CEREBELLAR ATROPHY

OPTIC CHIASMA

HYPERTROPHY

CLAVA (ENLARGEMENT OF GRACILE AND CUNEATE NUCLEUS

BY AXONAL SWELLING AND SPHEROIDS) 

HYPERINTENSITY (T2/ FLAIR)

CEREBELLAR CORTEX

MRI MAY BE NORMAL

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H-ABC (TUBB4A)

ATROPHY 

CEREBELUM 

PUTAMEN AND CAUDATE

HYPERINTENSITY (T2/ FLAIR)

DIFFUSE HYPOMYELINATION​

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CEREBELLUM/ TRACTS

GM2 GANGLIOSIDOSIS

ATROPHY

CEREBELLAR HEMISPHERE AND VERMIS

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NEURONAL CEROID LIPOFUSCINOSES

HYPOINTENSITY (T2)

THALAMI

ATROPHY

CEREBRAL CORTEX

CEREBELLUM

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ATAXIA TELENGIECTASIA (ATM)

ATROPHY 

INFERIOR VERMIS WITH GIANT CISTERNA MAGNA

CEREBELLAR HEMISPHERE

THIN SUPERIOR CEREBELLAR HEMISPHERE CORTEX

HYPERINTENSITY (T2/ FLAIR)

CONFLUENT CEREBRAL HYPERINTENSITY

HYPOINTENSITY (T2)

MULTIFOCAL T2 HYPOINTENSITY

HEMOSIDERIN RELATED TO CAPILLARY TELENGIECTASIA

AVOID CT SCAN

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ATAXIA WITH OCULOMOTOR APRAXIA (AOA) 

ATROPHY 

CEREBELLAR HEMISPHERE

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COENZYME Q10 DEFICIENCY

COQ8A DEFICIENCY MOST COMMON (ADCK3)

ATROPHY 

CEREBELLUM 

HYPERINTENSITY (T2/ FLAIR)

DENTATE/ PONS  

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MERRF

HYPERINTENSITY (T2/ FLAIR)

MEDIAL THALAMUS

DORSAL BRAIN STEM

LACTATE PEAK ON SPECTROSCOPY

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POLG1

HYPERINTENSITY (T2/ FLAIR)

INFERIOR OLIVARY NUCLEI

CEREBELLAR WHITE MATTER 

MCP/ DORSAL THALAMUS

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LEIGH SYNDROME

ATROPHY 

CEREBELUM 

HYPERINTENSITY (T2/ FLAIR)

DENTATE

PERIAQUEDUCTAL

PONTINE TEGMENTUM

MEDULLA OBLONGATA

POSTERIOR PUTAMEN

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SCA6 (CACNA1A)

ATROPHY 

CEREBELUM 

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SCA5 (SPTBN2)

ATROPHY 

CEREBELUM 

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POLR3B 

ATROPHY 

CEREBELLUM/ VERMIS

HYPERINTENSITY (T2/ FLAIR)

MCP

HYPOMYELINATION OF CEREBRAL AND CEREBELLUM

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PONTOCEREBELLAR HYPOPLASIA (PCH)

ATROPHY

PONS AND CEREBELLUM ATROPHY

CAUDATE ATROPHY

CORPUS CALLOSAL THINNING

HYPERINTENSITY (T2. FLAIR)

HYPOMYELINATION

PCH2 (TSEN10)  

DRAGON FLY MRI (CORONAL IMAGES)

SEVERE CEREBELLAR HEMISPHERE APLASIA

WITH SPARING OF VERMIS

PCH6 

VERMIS AND CEREBELLAR HEMISPHERE ATROPHY

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CONGENITAL DISORDER OF GLYCOSYLATION (GDC1a)

ATROPHY

CEREBELLUM

HYPERINTENSITY (T2)

DENTATE NUCLEUS

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COCKAYNE SYNDROME

ATROPHY

CEREBELLAR HEMISPHERE

CEREBELLUM

HYPERINTENSITY (T2/ FLAIR)

HYPOMYELINATION

CALCIFICATION

BASAL GANGLIA CALICIFICATION

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SPINAL CORD/ TRACTS DISORDERS

ARSACS (SACS)

HYPOINTENSITY (T2) 

PONS CENTRAL

HYPERINTENSITY (FLAIR)

HORIZONTAL PONS STRIATIONS (CST)

PERIPHERAL PONS HYPERINTENSITY

RIM OF HYPERINTENSITY AROUNF THALAMI

ATROPHY 

SUPERIOR VERMIS

SPINAL CORD

CORPUS CALLOSUM

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