Search on: FRAGILE X SYNDROME 
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Descriptor English:   Fragile X Syndrome 
Descriptor Spanish:   Síndrome del Cromosoma X Frágil 
Descriptor Portuguese:   Síndrome do Cromossomo X Frágil 
Synonyms English:   FRAXA Syndrome
FRAXE Syndrome
Martin-Bell Syndrome  
Tree Number:   C10.597.606.643.455.500
C16.131.260.800.300
C16.320.180.800.300
C16.320.322.500.500
C16.320.400.525.500
Definition English:   A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. MENTAL RETARDATION occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226) 
See Related English:   Chromosome Fragile Sites
Chromosome Fragility
Mental Retardation
Trinucleotide Repeat Expansion
 
History Note English:   91(83); was see under SEX CHROMOSOME ABNORMALITIES 1983-90 
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:   5735 
Unique Identifier:   D005600 

Occurrence in VHL:
 

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