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Hepatolenticular Degeneration
Hepatolenticular degeneration
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Hepatology
Hepatic transplant
Ceruloplasmin
Acute liver failure
Cirrhosis
Liver disease
Gaucher disease
Jaundice
Autosomal recessive disorders
Leukodystrophy, globoid cell
Tyrosinemias
Tay Sachs disease
Gaucher disease
Gastroenterology
Hemochromatosis
Hepatic transplant
Cirrhosis
Jaundice
Rare diseases
Menkes syndrome
Leukodystrophy, globoid cell
Tay Sachs disease
Gaucher disease
Genetic disorders
(9)
Hereditary sensory and autonomic neuropathies
Hyperostosis, cortical, congenital
Galactosemias
Huntington disease
Inherited disorder
Inherited disorder
Leukodystrophy, globoid cell
Tyrosinemias
Tay Sachs disease
Gaucher disease
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Neurological disorders
Hereditary sensory and autonomic neuropathies
Huntington disease
Diseases and disorders
(41)
Hemorrhagic thrombocythemia
Hand-Schul- ler-Christian disease
Haverhill fever
Intraparenchymal hemorrhage
Hansens Disease
Hansens Disease
Hereditary amyloidosis
Hemangioma
Hageman factor
Cerebral pseudosclerosis
Neurohepatic degeneration
Hereditary-sensory and autonomic neuropathy type iii
Lupus erythematosus, cutaneous
Hepatitis d, chronic
Physiologic nystagmus
Pseudosclerosis
Yellow nail syndrome
Hypertension, renovascular
Familial nephritis
Mitral valve prolapse
Hepatoeryt- hropoietic porphyria
Hyponatremia
Vaginitis
Hydronephrosis
Mastalgia
Gestational hypertension
Senescent
Hydrocephalus
Movement disorders
Dystonia
Leukodystrophy, globoid cell
Hereditary sensory and autonomic neuropathies
Hyperostosis, cortical, congenital
Galactosemias
Tyrosinemias
Huntington disease
Hemochromatosis
Cirrhosis
Menkes syndrome
Tay Sachs disease
Gaucher disease
Jaundice
more...
Lipid storage disorders
(14)
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Gangliosidosis
Gangliosidosis
Gaucher disease
Leukodystrophy, globoid cell
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Niemann–Pick disease
Sandhoff disease
Schindler disease
Tay Sachs disease
Wolman disease
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Symptoms
(20)
Dysmenorrhea
Abdominal distension
Delirium
Dementia
Difficulty walking
Difficulty walking
Hematemesis
Mental confusion
Slow movements
Speech disorder
Splenomegaly
Tremors of the arms or hands
Unpredictable and jerky movement
Weakness
Yellow skin
Seborrheic dermatitis
Painful menstruation
Uncontrollable movement
Hypertrophic scar
Mastalgia
Movement disorders
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Signs and tests
(20)
AST
Abdominal MRI
Abdominal x-ray
Albumin
Alt
Alt
Amino acid
Bilirubin
CBC
CT scan of the abdomen
Head CT scan
Head MRI
Hemolytic anemia
Liver biopsy
Necrosis
PT
PTT
Serum ceruloplasmin
Tremors
Uric acid
White blood cell count
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See also
(20)
Herniation of the brain
Highly conserved sequence
Harrington rod
Kayser-Fleischer rings
Heart sounds
Heart sounds
Vasospasm, intracranial
Spleen disorders
Wilson disease protein
Syprine
Trientine
Menorrhagia
Penicillamine
Copper metabolism
Anemia
Contracture
Hepatitis
Www.geneti- calliance.org
Www.wilson- sdisease.org
Wilson Wilson
Homogentisic acid oxidase
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