Kosmix
One sec... we're building Patient Experiences for
Canavan Disease
Canavan disease
: Patient-Experiences
Overview
Health Providers & Organizations
Main ›
Related in the Kosmos
?
Leukodystrophies
Krabbe disease
Adrenoleuk- odystrophy
Alexander disease
Pelizaeus-- merzbacher disease
Metachromatic leukodystrophy
Cerebrohepatorenal syndrome
Lysosomal storage diseases
(39)
Batten disease
Gaucher disease
Mucolipidosis IV
Mucopolysa- ccharidosis
Niemann Pick disease
Niemann Pick disease
Pompe disease
Tay Sachs disease
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Wolman disease
more...
Ashkenazi Jews topics
(91)
Ashkenazi Jewish
Bloom syndrome
Dor Yeshorim
Familial dysautonomia
Fanconi anemia
Fanconi anemia
Torsion dystonia
Agudat Yisrael
Ashkenazi Hebrew
Ashkenazi intelligence
Balabusta
Chassidei Ashkenaz
Chutzpah
Degel HaTorah
Fortress synagogue
GM2 gangliosidoses
Gaucher disease
Haplogroup G2c (Y-DNA)
Haplogroup K (mtDNA)
Haredi Judaism in Europe
Hasidic Judaism
Haskalah
History of the Jews in Galicia (Central Europe)
History of the Jews in Latin America
Jews and Judaism in Argentina
Jews and Judaism in Australia
Jews and Judaism in Austria
Jews and Judaism in Belarus
Jews and Judaism in Belgium
Jews and Judaism in Brazil
Jews and Judaism in Bulgaria
Jews and Judaism in Canada
Jews and Judaism in Chile
Jews and Judaism in Denmark
Jews and Judaism in Estonia
Jews and Judaism in France
Jews and Judaism in Galicia (Central Europe)
Jews and Judaism in Germany
Jews and Judaism in Honduras
Jews and Judaism in Hungary
Jews and Judaism in Iceland
Jews and Judaism in Ireland
Jews and Judaism in Italy
Jews and Judaism in Latvia
Jews and Judaism in Lithuania
Jews and Judaism in Mexico
Jews and Judaism in Norway
Jews and Judaism in Peru
Jews and Judaism in Poland
Jews and Judaism in Romania
Jews and Judaism in Russia
Jews and Judaism in Scotland
Jews and Judaism in Serbia
Jews and Judaism in South Africa
Jews and Judaism in Sweden
Jews and Judaism in Ukraine
Jews and Judaism in Venezuela
Jews and Judaism in Wales
Jews and Judaism in Zimbabwe
Jews and Judaism in the Czech Republic
Jews and Judaism in the Netherlands
Jews and Judaism in the Soviet Union
Jews and Judaism in the United Kingdom
Jews and Judaism in the United States
Khazars
Kitniyot
List of Jews born in the former Russian Empire
Maggid
Memorbuch
Misnagdim
Mucolipidosis
Mucolipidosis IV
Niemann Pick disease
Nusach Sefard
Oberlander Jews
Pemphigus
Rothschild banking family of England
Rothschild family
Sabbateans
Shtetls
Tay Sachs disease
The Thirteenth Tribe
Underground to Palestine
United Torah Judaism
Usher syndrome
Wimpel
Wooden synagogues
World Agudath Israel
Yekke
Yiddish
Yiddish language
Yiddishkeit
more...
Autosomal recessive disorders
(21)
Cerebrotendinous xanthomatosis
Very long-chain acyl coenzyme A dehydrogenase deficiency
Cystathioninuria
Spinal muscular atrophy type 1
Familial mediterranean fever
Familial mediterranean fever
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Cystinuria
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
Tay Sachs disease
Krabbe disease
Niemann Pick disease
Gaucher disease
Fanconi anemia
Mucolipidosis IV
Bloom syndrome
Familial dysautonomia
Metachromatic leukodystrophy
Batten disease
Pompe disease
Mucopolysa- ccharidosis
more...
Genetic disorders
(36)
Genetic diseases
Charcot-Marie Tooth Disease
Crouzonode- rmoskeletal syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Myotonic dystrophy
Myotonic dystrophy
Chromosome abnormalities
Coffin-lowry syndrome
Chronic granulomatous disease
Aicardi syndrome
Klinefelter syndrome
Tay Sachs disease
Krabbe disease
Niemann Pick disease
Gaucher disease
Adrenoleuk- odystrophy
Fanconi anemia
Mucolipidosis IV
Alexander disease
Bloom syndrome
Leukodystrophies
Pelizaeus-- merzbacher disease
Metachromatic leukodystrophy
Batten disease
Pompe disease
Cerebrotendinous xanthomatosis
Very long-chain acyl coenzyme A dehydrogenase deficiency
Cystathioninuria
Spinal muscular atrophy type 1
Familial mediterranean fever
Cerebrohepatorenal syndrome
Mucopolysa- ccharidosis
Long-chain 3-hydroxya- cyl-coenzyme A dehydrogenase deficiency
Torsion dystonia
Cystinuria
Carnitine palmitoylt- ransferase I deficiency
Carnitine palmitoylt- ransferase II deficiency
more...
Diseases and disorders
(57)
Canavan-van bogaert-bertrand disease
Vocal tic disorder
Leukodystrophy
Chemical pneumonitis
Cancer of the kidney
Cancer of the kidney
Macrocephaly
Cancer of the skin
Hypotonia
Feeding difficulties
Chromosome 5p- syndrome
Alzheimer disease type 2
Progressive supranuclear palsy
Dysmyelination
Glycogen storage disease
Coccidioidomycosis
Optic atrophy
Demyelination
Congenital facial diplegia
Complex regional pain syndromes
Cushing syndrome
Megalocephaly
Infant botulism
Cerebral gigantism
Phytanic acid storage disease
Chronic Progressive External Ophthalmoplegia
Hypomyelination
Neurological disorders
Menkes syndrome
Temporal arteritis
Kernicterus
Tay Sachs disease
Krabbe disease
Niemann Pick disease
Gaucher disease
Fanconi anemia
Mucolipidosis IV
Alexander disease
Bloom syndrome
Familial dysautonomia
Charcot-Marie Tooth Disease
Pelizaeus-- merzbacher disease
Metachromatic leukodystrophy
Batten disease
Pompe disease
Cerebrotendinous xanthomatosis
Spondyloep- imetaphyseal dysplasia, Strudwick type
Spinal muscular atrophy type 1
Myotonic dystrophy
Chromosome abnormalities
Familial mediterranean fever
Cerebrohepatorenal syndrome
Mucopolysa- ccharidosis
Coffin-lowry syndrome
Chronic granulomatous disease
Cystinuria
Carnitine palmitoylt- ransferase II deficiency
Klinefelter syndrome
more...
Symptoms
(8)
Reflux
Seizure
Abnormal muscle tone
Inability to walk
Decreased muscle tone
Decreased muscle tone
Macrocephaly
Hypotonia
Feeding difficulties
more...
Signs and tests
CSF chemistry
Head CT
Head MRI scan
Joint stiffness
Urine chemistry
See also
(20)
Cerebellar herniation
Cancer of the bile ducts
Aspartoacylase
Chlamydia infection
Myrtelle Canavan
Myrtelle Canavan
N-acetylaspartic acid
Myelin sheath
Mutation analysis
Chromosome analysis
Lipoprotein lipase deficiency, familial
Paola Leone
Aspartic acid
Canavan
Central nervous system
Enzyme
The Myelin Project
The Stennis Foundation
White matter of the brain
Www.canava- nfoundation.org
Spongy tissue
more...
more categories...
