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Globoid Cell Leukodystrophy
Globoid cell leukodystrophy
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Leukodystrophies
Adrenoleuk- odystrophy
Alexander disease
Metachromatic leukodystrophy
Canavan disease
Pelizaeus-- Merzbacher disease
Zellweger syndrome
Lipid storage disorders
(13)
Gangliosidosis
Gaucher disease
Tay Sachs disease
Wolman disease
Fabry disease
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Multiple sulfatase deficiency
Niemann-Pick disease, type C
Niemann–Pick disease
Sandhoff disease
Schindler disease
more...
Lysosomal storage diseases
(39)
Galactosam- ine-6-sulfatase deficiency
Lipidosis
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher disease
Glycogen storage disease type II
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Lysosomal storage disease
Metachromatic leukodystrophy
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay Sachs disease
Wolman disease
more...
Metabolic disorders
(59)
Galactosemias
Activated protein C resistance
Adenosine deaminase deficiency
Albinism
Alcohol flush reaction
Alcohol flush reaction
Antithrombin III deficiency
Baker IDI Heart and Diabetes Institute
Blue diaper syndrome
Childhood obesity
Congenital disorder of glycosylation
Congenital hyperinsulinism
Crigler-Najjar syndrome
Diagnostic fast
Disaccharidase
Disorders of calcium metabolism
Ectopic calcification
Farber disease
Fructose malabsorption
GM1 gangliosidoses
GM2 gangliosidoses
Galactosemic cataract
Gangliosidosis
Gaucher disease
Glycogen storage disease type 0
Hereditary fructose intolerance
Homocystinuria
Hyperglycemia
Hyperinsulinemic hypoglycemia
Hyperinsulinism
Hypoglycemia
Inborn errors of metabolism
Ketotic hypoglycemia
Lactose intolerance
Lipid storage disorders
List of causes of hypoglycemia
Metab-L
Methemoglobinemia
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Obesity
Obesogen
Pickardt syndrome
Pycnodysostosis
Refeeding syndrome
Richner Hanhart syndrome
Rotor syndrome
Salicylate sensitivity
Schindler disease
Selfish Brain Theory
Sitosterolemia
Stress hyperglycemia
Sucrose intolerance
Tay Sachs disease
Triosephosphate isomerase deficiency
Urbach–Wiethe disease
Urea cycle disorder
Winchester syndrome
Wolman disease
more...
Inborn errors of metabolism
(8)
Glycogen storage disease type v
Phytanic acid storage disease
Fucosidosis
Pyruvate kinase deficiency
Lipidosis
Lipidosis
Galactosemias
Wolman disease
Lysosomal storage diseases
more...
Autosomal recessive disorders
(11)
Thrombasthenia
Copper toxicosis
Glycogen storage disease type v
Gaucher disease
Metachromatic leukodystrophy
Metachromatic leukodystrophy
Lipidosis
Galactosam- ine-6-sulfatase deficiency
Gangliosidosis
Fucosidosis
Wolman disease
Tay Sachs disease
more...
Rare diseases
(12)
Goodpastures Syndrome
Thrombasthenia
Gaucher disease
Metachromatic leukodystrophy
Lipidosis
Lipidosis
Galactosam- ine-6-sulfatase deficiency
Gangliosidosis
Alexander disease
Fucosidosis
Copper toxicosis
Wolman disease
Tay Sachs disease
more...
Genetic disorders
(24)
Ileocolitis
Hyperostosis, cortical, congenital
Luschka-Magendie foramina atresia
Hereditary sensory and autonomic neuropathies
Loken Senior syndrome
Loken Senior syndrome
Kniest dysplasia
Klinefelter syndrome
Gluten sensitive enteropathy
Thrombasthenia
Glycogen storage disease type v
Adrenoleuk- odystrophy
Gaucher disease
Metachromatic leukodystrophy
Lipidosis
Galactosemias
Galactosam- ine-6-sulfatase deficiency
Gangliosidosis
Leukodystrophies
Alexander disease
Fucosidosis
Pyruvate kinase deficiency
Copper toxicosis
Wolman disease
Tay Sachs disease
more...
Diseases and disorders
(60)
Gonococcal
Glomerulonephritis, membranopr- oliferative
Granulomatous
Gonadotropin deficiency
Gyrate atrophy
Gyrate atrophy
Mesangial proliferative glomerulonephritis
Bacteremia
Gluten enteropathy
Post-streptococcal glomerulonephritis
Glossopharyngeal neuralgia
Glucose 6 phosphate dehydrogenase deficiency
Glossopharyngeal nerve diseases
Lupus erythematosus, cutaneous
Galactosyl- ceramidase deficiency disease
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lancereaux- -Mathieu-Weil Spirochetosis
Progressive sclerosing poliodystrophy
Physiologic nystagmus
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Leukodystrophy
Intervertebral disk displacement
Keratoconj- unctivitis sicca
Rosenthal syndrome
Sphingolipidosis
Brachial plexus neuropathies
Optic neuropathy, ischemic
Demyelination
Leukoencephalopathy with neuroaxonal spheroids
Leukemia, hairy cell
Gigantism
Goodpastures Syndrome
Thrombasthenia
Ileocolitis
Hyperostosis, cortical, congenital
Hereditary sensory and autonomic neuropathies
Gaucher disease
Phytanic acid storage disease
Metachromatic leukodystrophy
Lipidosis
Kniest dysplasia
Galactosemias
Galactosam- ine-6-sulfatase deficiency
Gangliosidosis
Alexander disease
Fucosidosis
Pyruvate kinase deficiency
Copper toxicosis
Wolman disease
Klinefelter syndrome
Lysosomal storage diseases
Tay Sachs disease
Gluten sensitive enteropathy
more...
Inflammations
Glossitis
Glomerulonephritis, membranous
Glomerulonephritis, membranopr- oliferative
Ileocolitis
Dog diseases
Craniomandibular osteopathy
Ocular melanosis
Portosystemic shunt
Progressive retinal atrophy
Lancereaux- -Mathieu-Weil Spirochetosis
Keratoconj- unctivitis sicca
Symptoms
Decerebrate posturing
Failure to thrive
Seizure
Keratoconj- unctivitis sicca
Signs and tests
CSF albumin
MRI of the head
Nerve conduction study
Abnormal posturing
See also
(20)
Glucuronyl transferase
Granulomatous thyroiditis
Glucocerebroside
Galactosyl- ceramidase
Galactocerebroside
Galactocerebroside
People of Scandinavian descent
Vasospasm, intracranial
Hirayama syndrome
Myelin
Grapefruit juice
Myoclonic Encephalopathy of infants
Guaiac smear test
Amniocentesis
Autosomal recessive pattern
Central nervous system
Chorionic villus sampling
Genetic counseling
Jim Kelly
The Myelin Project
The Stennis Foundation
more...
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