Canavanine
L-(+)-(S)-Canavanine is a non-proteinogenic amino acid of certain leguminous plants. It is structurally related to the proteinogenic amino acid, L-arginine.
Canavan disease (CD)
Canavan disease is a rare and fatal inherited disease that leads to the progressive degeneration of the brain and nervous system.
Canavan disease, also called Canavan-Van Bogaert-Bertrand disease, aspartoacylase deficiency or aminoacylase 2 deficiency, is an autosomal recessive degenerative disorder that causes progressive damage to nerve cells in the...
Canavan disease
Definition
Canavan disease is an inherited condition that affects the breakdown and use (metabolism) of aspartic acid.
Canavan disease
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Canavan Disease Causes, Symptoms and Treatment and Related Disorders ...
Canavan disease
Alternate Names : Spongy degeneration of the brain, Aspartoacylase deficiency
Definition ...
Canavan Disease
National Organization for Rare Disorders, Inc.
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Canavan Disease
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What is Canavan disease?
Canavan disease is an inherited disorder that causes progressive damage to nerve cells in the brain. This disease is one of a group of genetic disorders called leukodystrophies.
Canavan disease is an inherited condition that affects the breakdown and use (metabolism) of aspartic acid.
Alternative Names
Spongy degeneration of the brain; Aspartoacylase deficiency ...
Canavan disease is an inherited neurological disease. It affects the myelin, or sheaths surrounding the nerves in the brain. It is one of a group of genetic neurological disease known as the leukodystrophies.
Canavan disease - caused by mutations in the ASPA gene More than 55 mutations in the ASPA gene are known to cause Canavan disease.
Canavan disease is caused by a deficiency of the enzyme aspartoacylase. This leads to increased excretion of a substance (its substrate) called N-acetylaspartic acid (NAA) in the urine.
Canavan disease
A neurodegenerative disease characterized by lack of the aspartoacylase enzyme, which is critical for central nervous system development and function.
Canavan disease: A severe progressive inherited (genetic) disorder of the central nervous system (CNS). The signs of Canavan disease usually appear when the children are between 3 and 6 months of age.
Canavaninosuccinic Acid
PK´
Apparent Value Of A PK; Negative Logarithm Of The Dissociation Constant Of An Acid ...
Canavan disease
DNA analysis to detect most common mutations
CVS or amniocentesis for DNA analysis ...
Canavan disease ... blindness
Canavan leukodystrophy ... blindness
CAR syndrome ... loss of peripheral vision, photosensitivity, reduced visual acuity, reduced visual acuity, vision loss, vision loss, night blindness, night blindness ...
Canavan Disease
Canavan's Leukodystrophy
Canavan-Van Bogaert-Bertrand Disease
Cancell/Cantron/Protocel (PDQ®): Complementary and alternative medicine - Health Professional Information [NCI] ...
with selected letter: 1330 1 2 3 4 5 6 7 8 9 10 11 12 13 14 Current page: 9Disease, acute respiratory Disease, Addison Disease, adult celiac Disease, alveolar hydatid Disease, Bernard-Soulier Disease, Bornholm Disease, Brill-Zinsser Disease, Canavan ...
Canavan disease
Cancer
Carbamyl Phosphate Synthase see Urea Cycle disorders
Carbohydrate Deficient Glycoprotein syndrome see Congenital disorders of Glycosylation
Cardiofaciocutaneous syndrome
Cardiomyopathies ...
Canavan disease Opens New Window. This disease gradually destroys brain tissue.
Cystic fibrosis Opens New Window. This disease causes very thick mucus in the lungs and problems with digesting food.
Familial dysautonomia Opens New Window (FD).
Canavan disease
Congenital hypothyroidism
Congenital cerebellar ataxia
Down syndrome
Familial dysautonomia (Riley-Day syndrome)
Hypervitaminosis
Infant botulism
Kernicterus (brain damage due to severe jaundice)
Klinefelter syndrome ...
Arthritis mutilans, DFPP (CFSAN), DMSO, Determination, Blood Pressure, Disease, Forbes, Distal Renal Tubular Acidosis, Dysmetrias, Ethics Committee, Factors, Colicin, Familial Form of Canavan Disease, Flaviviridae Infections, Formamides, ...
Pelizaeus-Merzbacher disease
Canavan disease
Childhood ataxia with central nervous system hypomyelination (CACH, also called vanishing white matter disease)
Alexander disease
Refsum disease
Cerebrotendinous xanthomatosis ...
Benign familial macrocephaly (family tendency toward large head size)
Canavan disease
Hurler syndrome
Hydrocephalus (congenital, post-traumatic, or obstructive)
Intracranial bleeding
Morquio syndrome ...
Alfalfa sprouts and legumes, to a lesser extent, should also be avoided as the constituent L-canavanine causes SLE-like diseases in primates. [Acta Medica Scandinavica 1984;216: pp. 67-274] Peas and lima beans are alright to eat in this regard.
autoimmune (Multiple sclerosis, Neuromyelitis optica, Schilder's disease) Â- hereditary (Adrenoleukodystrophy, Alexander, Canavan, Krabbe, ML, PMD, VWM, MFC, CAMFAK syndrome) Â- Central pontine myelinolysis Â- Marchiafava-Bignami disease Â- Alpers' ...
Specific leukodystrophies include metachromatic leukodystrophy, Krabbé disease, adrenoleukodystrophy, Pelizaeus-Merzbacher disease, Canavan disease, ...
Partial (focal) seizure
Peritoneal fluid analysis
Spine MRI
Canavan disease
PBG test
Aging changes in the senses
Developmental disorders of the female reproductive tract
Drug-induced hypertension
Energy preservation ...
Canavan's disease (spongy degeneration) - this form causes abnormal myelin growth. The typical form is characterised by poor head control, decreased tone, regression and a markedly enlarged head. Eventually the decreased tone changes to stiffness.
 See also: Canavan disease, Symptom, Cancer, Autosomal recessive, Stroke
  
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