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5,639 Possible Causes for Ataxia, MRI Shows Increased Connective Tissue and Fat, Onset of Symptoms in First or Second Decade of Life

  • Limb-Girdle Muscular Dystrophy Type 2L

    The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation.[icd10data.com] Primary ciliary dyskinesia Short rib-polydactyly syndrome 3 Asphyxiating thoracic dysplasia 3 Other Tauopathy Cavernous venous malformation Membrane Spectrin : Spinocerebellar ataxia[en.wikipedia.org] Seizures, ataxia, and ocular abnormalities can occur. LGMD2T - GDP-mannose pyrophosphorylase B (GMPPB ) mutation.[emedicine.medscape.com]

  • Hallervorden-Spatz Syndrome

    There is an early onset classic form with symptoms of extrapyramidal disease beginning in the first decade of life and rapid progression to loss of ambulation in about 15[disorders.eyes.arizona.edu] The patient presented with a slowly progressive illness with seizures, extrapyramidal symptoms, cerebellar ataxia, dementia, spasticity, myoclonic movements and a severe demyelinating[ncbi.nlm.nih.gov] Although rare, cerebellar ataxia, behavioural abnormalities, parkinsonism and apraxia of eyelid opening were exclusively seen in late onset patients.[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Huntington's Disease

    However, in some families a juvenile form of HD has been seen with an onset of symptoms in the first or second decades of life.[encyclopedia.com] We screened 89 patients with a Huntington's disease-like phenotype without the HD-gene mutation and 178 patients with genetically unclassified cerebellar ataxia for the mutation[ncbi.nlm.nih.gov] The authors highlight the importance of suspecting HD in the aetiology of spinocerebellar ataxias when dementia is a prominent feature in the proband or their family.[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Hereditary Areflexic Dystasia

    Age of onset is in the second and third decades of life and rarely in the first. Recovery is usually complete and begins weeks to months after the onset of symptoms.[emedicine.medscape.com] Cerebellar ataxia, early-onset Cerebellar ataxia, late-onset Drug-induced cerebellar ataxia Early onset cerebellar ataxia Early onset cerebellar ataxia with essential tremor[icd9data.com] 2013 ICD-9-CM Diagnosis Code 334.3 Other cerebellar ataxia Short description: Cerebellar ataxia NEC.[icd9data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Hypertrophic Interstitial Neuropathy

    […] of symptoms usually in the second decade Progression is slower than in type 1 Nerve conduction studies are usually normal, but electromyography shows evidence of denervation[quizlet.com] Synonym(s): interstitial hypertrophic neuropathy Roussy-Lévy disease - a type of cerebellar ataxia regularly associated with wasting of the calves and intrinsic muscles of[medical-dictionary.thefreedictionary.com] , ataxy, ataxic R27.0 ICD-10-CM Diagnosis Code R27.0 Ataxia, unspecified 2016 2017 2018 2019 Billable/Specific Code Type 1 Excludes ataxia following cerebrovascular disease[icd10data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Friedreich Ataxia

    Most affected people become wheelchair dependent by the second or third decade of life.[web.archive.org] Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.[doi.org] Convert to ICD-10-CM : 334.0 converts approximately to: 2015/16 ICD-10-CM G11.1 Early-onset cerebellar ataxia Approximate Synonyms Cervical neuromuscular scoliosis due to[icd9data.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Hereditary Angioedema

    Onset of clinical symptoms occurred in the first decade of life in 11 (8%) patients, in the second decade in 60 (43.5%) patients, in the third decade in 22 (15.9%) patients[aacijournal.biomedcentral.com] Episodes of severe headaches, visual disturbances (eg, blurred vision, diplopia), and ataxia have been reported.[emedicine.medscape.com] Onset of clinical symptoms In a series of 138 patients, the mean age at onset of the disease was 26.8 years (SD /- 14.9 years, range 1 to 68 years) [ 12 ].[aacijournal.biomedcentral.com]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Hereditary Spastic Paraplegia

    Clinical Correlations: Spastic paraplegia 7 may have its onset in the second decade of life but sometimes much later.[disorders.eyes.arizona.edu] INTRODUCTION: The combination of cerebellar ataxia and spasticity is common.[ncbi.nlm.nih.gov] Criteria for hereditary ataxia The following groups were included: subjects with progressive cerebellar ataxia and positive family history or confirmed genetic diagnosis;[dx.doi.org]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Kearns-Sayre Syndrome

    Signs and symptoms [ edit ] Individuals with KSS present initially in a similar way to those with typical CPEO. Onset is in the first and second decades of life.[en.wikipedia.org] We review the differential diagnosis of cerebellar ataxia with vision loss secondary to retinal pigmentary dystrophy.[ncbi.nlm.nih.gov] In addition to the main clinical symptoms, at least one of the following is also often present: heart block, cerebellar ataxia, or cerebrospinal fluid (CSF) protein content[orpha.net]

    Missing: MRI Shows Increased Connective Tissue and Fat
  • Vitamin B12 Deficiency

    A previously healthy 7-year-old Caucasian boy was hospitalised for evaluation of acute ataxia and failure to thrive, initially suspicious for an intracranial mass.[ncbi.nlm.nih.gov] We describe a patient who manifested with acute onset of language dysfunction, chorea and ataxia.[ncbi.nlm.nih.gov] We describe an elderly patient with vitamin B12 deficiency who presented cognitive dysfunction, peripheral polyneuropathy and sensory ataxia, and whose first clinical manifestation[ncbi.nlm.nih.gov]

    Missing: MRI Shows Increased Connective Tissue and Fat Onset of Symptoms in First or Second Decade of Life

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