serw-MX  [xml]  

 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10. Brain Diseases, Metabolic, Inborn .
C10. Hereditary Central Nervous System Demyelinating Diseases .
C10. Canavan Disease .
C10.228.140.695 Leukoencephalopathies .
C10.228.140.695.625 Hereditary Central Nervous System Demyelinating Diseases .
C10.228.140.695.625.375 Canavan Disease .
C10.314 Demyelinating Diseases .
C10.314.400 Hereditary Central Nervous System Demyelinating Diseases .
C10.314.400.375 Canavan Disease .
C10.574 Neurodegenerative Diseases .
C10.574.500 Heredodegenerative Disorders, Nervous System .
C10.574.500.300 Canavan Disease .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.703 Pregnancy Complications .
C13.703.572 Perinatal Death .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.400 Heredodegenerative Disorders, Nervous System .
C16.320.400.150 Canavan Disease .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C16.320.565.189.362.375 Canavan Disease .
C16.614 Infant, Newborn, Diseases .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.132.100.362.375 Canavan Disease .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.362 Hereditary Central Nervous System Demyelinating Diseases .
C18.452.648.189.362.375 Canavan Disease .
C23 Pathological Conditions, Signs and Symptoms .
C23.550 Pathologic Processes .
C23.550.260 Death .
C23.550.260.865 Perinatal Death .
M01 Persons .
M01.060 Age Groups .
M01.060.703 Infant .
M01.060.703.520 Infant, Newborn .
SP4 Environmental Health .
SP4.001 Health .
SP4.001.012 Environmental Illness .
SP4.001.012.133 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
 Synonyms & Historicals
Infant, Newborn, Diseases .
Neonatal Diseases .
Disease, Neonatal .
Diseases, Neonatal .
Neonatal Disease .
Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. .
Canavan Disease .
ACY2 Deficiency .
ASP Deficiency .
ASPA Deficiency .
Aminoacylase 2 Deficiency .
Aspartoacylase Deficiency .
Canavan Disease, Familial Form .
Canavan Disease, Infantile .
Canavan Disease, Juvenile .
Canavan Disease, Neonatal .
Canavan Disease, Sporadic Form .
Canavan Disease, Type I .
Canavan Disease, Type II .
Canavan Disease, Type III .
Canavan-van Bogaert-Bertrand Disease .
Deficiency Disease, Aspartoacylase .
Familial Form of Canavan Disease .
Infantile Canavan Disease .
Juvenile Canavan Disease .
Leukodystrophy, Spongiform .
Neonatal Canavan Disease .
Spongy Degeneration Of Central Nervous System .
Spongy Degeneration of Infancy .
Spongy Degeneration of White Matter In Infancy .
Spongy Degeneration of the Brain .
Spongy Degeneration of the Central Nervous System .
Spongy Disease of Central Nervous System .
Spongy Disease of White Matter .
Sporadic Form of Canavan Disease .
Type I Canavan Disease .
Type II Canavan Disease .
Type III Canavan Disease .
Van Bogaert-Bertrand Syndrome .
Von Bogaert-Bertrand Disease .
Canavan van Bogaert Bertrand Disease .
Disease, Canavan .
Disease, Canavan-van Bogaert-Bertrand .
Disease, Von Bogaert-Bertrand .
Spongiform Leukodystrophy .
Syndrome, Van Bogaert-Bertrand .
Van Bogaert Bertrand Syndrome .
Von Bogaert Bertrand Disease .
Canavan-van Bogaert-Bertrand Disease .
Leukodystrophy, Spongiform .
Spongy Disease of White Matter .
A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. Aspartoacylase deficiency leads to an accumulation of N-acetylaspartate in astrocytes. Inheritance may be autosomal recessive or the illness may occur sporadically. This illness occurs more frequently in individuals of Ashkenazic Jewish descent. The neonatal form features the onset of hypotonia and lethargy at birth, rapidly progressing to coma and death. The infantile form features developmental delay, DYSKINESIAS, hypotonia, spasticity, blindness, and megalencephaly. The juvenile form is characterized by ATAXIA; OPTIC ATROPHY; and DEMENTIA. (From Adams et al., Principles of Neurology, 6th ed, p944; Am J Med Genet 1988 Feb;29(2):463-71) .
Infant, Newborn .
Newborns .
Infants, Newborn .
Neonates .
Newborn .
Newborn Infant .
Newborn Infants .
Neonate .
An infant during the first 28 days after birth. .
Perinatal Death .
Neonatal Death .
Death, Neonatal .
Death, Perinatal .
Deaths, Neonatal .
Deaths, Perinatal .
Neonatal Deaths .
Perinatal Deaths .
The death of a FETUS of GESTATIONAL AGE 28 weeks or more, or the death of a live-born INFANT less than 28 days of age. .
Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
Disorders, Congenital .
Congenital Disorder .
Disorder, Congenital .
Congenital Disorders .
Neonatal Diseases and Abnormalities .
Diseases existing at birth and often before birth, or that develop during the first month of life (INFANT, NEWBORN, DISEASES), regardless of causation. Of these diseases, those characterized by structural deformities are termed CONGENITAL ABNORMALITIES. .