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3,970 Possible Causes for Cerebellar Gait Ataxia, Hepatomegaly, Nocturnal Leg Cramp

  • Chronic Alcoholism

    Hepatomegaly (in chronic alcoholic liver disease the liver is shrunken). Ascites; gonadal atrophy. Atrial fibrillation and cardiomyopathy.[] The cause of the alcoholic gait is brain damage called alcoholic cerebellar ataxia.[] Characteristic ultrasonographic findings include a hyperechoic liver with or without hepatomegaly.[]

  • Pernicious Anemia

    Some people with Pernicious Anemia may have an abnormally enlarged liver (hepatomegaly) or spleen (splenomegaly).[] It causes ataxia of stance and gait with relative sparing of the arms. It has an insidious onset and a subacute or chronic course.[] Hepatomegaly and splenomegaly may be present.[]

  • Hypoglycemia

    An infant presented with short history of jaundice and irritability, examination showed soft hepatomegaly.[] Hepatomegaly. Response to glucagon is intact. Patients can be ketotic.[] Subsequently fasting hypoketotic hypoglycemia occurred without permanent hepatomegaly or hyperlipidemia.[]

    Missing: Cerebellar Gait Ataxia
  • Restless Legs Syndrome

    All patients have gait ataxia and the majority have lower limb ataxia.[] Two common causes of pain or discomfort in legs are nocturnal leg cramps (NLC) and restless leg syndrome (RLS).[] Leg pain and discomfort are common complaints in any primary physician's clinic.[]

    Missing: Hepatomegaly
  • Toxoplasmosis

    […] common encephalomyelitis, retinochoroiditis, intracranial calcification and hydrocephalus to the non-specific symptoms of acute infection such as convulsion, splenomegaly, hepatomegaly[] The authors report one rare case in a 50-year-old HIV-infected male patient who presented with clipped speech, gait ataxia and incoordination.[] There may be ventriculomegaly, CNS calcifications, placental changes, hepatomegaly, splenomegaly, ascites and pericardial or pleural effusion [ 3 ] .[]

    Missing: Nocturnal Leg Cramp
  • Hemochromatosis

    […] transferrin saturation (TS); ALT; AST; GGT; elevated C-reactive protein; ß-thalassemia; neutrophils; lymphocytes; monocytes; platelets; metacarpophalangeal joint hypertrophy; hepatomegaly[] […] difficulties, cerebellar ataxia, and extrapyramidal dysfunction.[] Eight of the 16 homozygous subjects had clinical findings that were consistent with the presence of hereditary hemochromatosis, such as hepatomegaly, skin pigmentation, and[]

    Missing: Nocturnal Leg Cramp
  • Peripheral Neuropathy

    All patients have gait ataxia and the majority have lower limb ataxia.[] GA is usually of insidious onset; however, it can also be rapidly progressive mimicking paraneoplastic cerebellar degeneration. Gaze-evoked nystagmus is common.[]

    Missing: Hepatomegaly
  • Hyperthyroidism

    On physical examination at admission, she was found to have jaundice and hepatomegaly. Laboratory data show cholestasis and protein-losing enteropathy.[] […] of the following: fever, marked weakness and muscle wasting, extreme restlessness with wide emotional swings, confusion, psychosis, coma, nausea, vomiting, diarrhea, and hepatomegaly[]

    Missing: Cerebellar Gait Ataxia
  • Alcohol Dementia

    […] of equilibrium, inco-ordination of gait, dysdiadochokinesis, limb ataxia or dysarthria. c) Altered mental state, for example, mental sluggishness, apathy or impaired awareness[] Caine criteria – two of the following four should be present. a) Ocular abnormality, for example, nystagmus or ophthalmoplegia. b) Cerebellar dysfunction, for example, loss[]

    Missing: Nocturnal Leg Cramp
  • Parkinson's Disease

    Clinical features include hepatomegaly with or without splenomegaly, jaundice, fat and fat-soluble vitamin malabsorption, and mild steatorrhea.[] Neonates with 3-β-hydroxy-C 27 -steroid oxidoreductase deficiency show hepatomegaly, mild steatorrhea, elevated serum ALT and AST, hyperbilirubinemia, and normal serum γ-glutamyl[]

    Missing: Cerebellar Gait Ataxia

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