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1,766 Possible Causes for Cerebellar Sign, Microcephaly (2-3 SD), Poor Coordination of the Lower Extremity

Did you mean: Cerebellar Sign, Microcephaly (2-3 SD, Poor Coordination of the Lower Extremity

  • Dysequilibrium Syndrome

    Microcephaly (-3 to -4 SD below the mean) has been reported in a few affected individuals. Life span.[] The characteristic finding on MRI is the "molar tooth sign" in which hypoplasia of the cerebellar vermis and accompanying brain stem abnormalities resemble a tooth.[] Short stature (height just below the 2 nd centile) is a feature in a few affected individuals. Deep tendon reflexes in the lower extremities tend to be brisk.[]

  • Cerebellar Neoplasm

    signs Radiology description Well circumscribed Hyperintense on pre contrast T1 weighted images due to lipid content Heterogeneous contrast enhancement Minimal edema Radiology[] Patients with a cerebellar lesion often present with a headache and signs of cerebellar dysfunction.[] ENG or rotatory chair testing may show specific signs of a cerebellar disorder.[]

    Missing: Microcephaly (2-3 SD)
  • Acute Cerebellar Ataxia

    Disorders of the blood vessels that supply blood to the cerebellum can also cause acute cerebellar ataxia. WHAT ARE SIGNS OF ACUTE CEREBELLAR ATAXIA?[] Abstract Acute Cerebellar Ataxia (ACA) is not infrequent disorder in childhood characterized by sudden onset of such cerebellar signs as truncal ataxia, dysmetria, tremors[] Severe cases of cerebellitis represent the other end of the spectrum, presenting with acute cerebellar signs often overshadowed by alteration of consciousness, focal neurological[]

    Missing: Microcephaly (2-3 SD)
  • Hereditary Cerebellar Degeneration

    Syndromes of cerebellar degeneration typically manifest as subacute or chronic cerebellar neurological signs.[] Autosomal dominant cerebellar ataxia type III produces relatively pure cerebellar signs.[] A relatively important one is sporadic Creutzfeldt-Jakob disease that can present with predominantly cerebellar signs [ 8 ].[]

    Missing: Microcephaly (2-3 SD)
  • Ataxia Telangiectasia

    Neurologic evaluation revealed minimal hypotonia and wide-based gait, without other signs of cerebellar dysfunction.[] The latter is suggested by an earlier onset of signs, the lack of cerebellar atrophy, and the absence of ataxia and ocular telangiectases on initial presentation.[] Children with AT between ages 1 and 4 may show signs of : Progressive cerebellar dysfunction, such as slurred speech Oculomotor apraxia (difficulty moving the eyes from side[]

    Missing: Microcephaly (2-3 SD)
  • Friedreich Ataxia

    The proband had cerebellar and pyramidal signs with distal sensory loss but preserved reflexes. The youngest sibling denied symptoms but had mild cerebellar signs.[] Ataxia Friedreich Ataxia Dyskinesias Neurologic Manifestations Nervous System Diseases Signs and Symptoms Cerebellar Diseases Brain Diseases Central Nervous System Diseases[] RESULTS: Brain imaging showed cerebellar degeneration in the eldest sibling but not in the other siblings.[]

    Missing: Microcephaly (2-3 SD)
  • Alcoholic Cerebellar Degeneration

    Nine of the 14 patients (Group A) had clinical signs of alcoholic cerebellar degeneration, and the remaining 5 (Group B) did not have signs of alcoholic cerebellar degeneration[] Syndromes of cerebellar degeneration typically manifest as subacute or chronic cerebellar neurological signs.[] Males females, Scanning speech and nystagmus unusual, Gait ataxia and postural instability more evident than the other cerebellar signs seen with more lateral cerebellar disease[]

    Missing: Microcephaly (2-3 SD)
  • Spinocerebellar Ataxia Type 5

    Poor Co-ordination- The function of upper and lower extremity muscles are affected, because of lack of normal coordination.[] Non-cerebellar signs such as facial myokimia, resting tremor, writer's cramp, impaired vibration sense and brisk deep tendon reflexes have been reported in some patients.[] Term Name: spinocerebellar ataxia type 5 Search Ontology: Synonyms: Definition: An autosomal dominant cerebellar ataxia that is characterized by the early-onset of cerebellar[]

    Missing: Microcephaly (2-3 SD)
  • Cerebellar Disease

    Abstract Ocular signs of cerebellar disease have been increasingly appreciated with the advent of means for quantitative recording of eye movements.[] MS also causes optic neuritis which leads to optic atrophy What are the signs of cerebellar disease DANISH T Dysdiadochokinesis Ataxia - broad based gait falling to side of[] Tandem gait The cerebellar patient will not be able to walk heel-to-toe. A sign of anterior cerebellar lobe dysfunction.[]

    Missing: Microcephaly (2-3 SD)
  • Helsmoortel-van der Aa Syndrome

    SCA8 SCA-8 is a slowly progressive ataxia resulting in poor coordination of limbs, especially lower extremities, and poor coordination of gait and speech.[] A common finding in microcephaly is also short stature, typically between -1 SD and -2 SD and in Seckel syndrome it ranges between -4 and -12 SD 3.[] […] retardation syndrome Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome Autosomal recessive cerebellar ataxia-saccadic intrusion[]

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