Search on: RETT SYNDROME 
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Descriptor English:   Rett Syndrome 
Descriptor Spanish:   Síndrome de Rett 
Descriptor Portuguese:   Síndrome de Rett 
Synonyms English:   Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome
Cerebroatrophic Hyperammonemia  
Tree Number:   C10.574.500.775
C10.597.606.643.455.937
C16.320.322.500.937
C16.320.400.525.937
C16.320.400.700
F03.550.325.412
Definition English:   An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199) 
See Related English:   Mental Retardation
 
History Note English:   90 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
ultrastructure urine
ultrasonography veterinary
virology  
Record Number:   24868 
Unique Identifier:   D015518 

Occurrence in VHL:
 

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