Search on: CITRULLINEMIA 
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Descriptor English:   Citrullinemia 
Descriptor Spanish:   Citrulinemia 
Descriptor Portuguese:   Citrulinemia 
Synonyms English:   Argininosuccinate Synthase Deficiency Disease  
Tree Number:   C10.228.140.163.100.175
C16.320.565.100.340
C16.320.565.189.175
C18.452.132.100.175
C18.452.648.100.340
C18.452.648.189.175
Definition English:   A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neonates, clinical manifestations include lethargy, hypotonia, and SEIZURES. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ATAXIA, behavioral changes, and DYSARTHRIA. (From Menkes, Textbook of Child Neurology, 5th ed, p49) 
See Related English:   Argininosuccinate Synthase
 
History Note English:   2000 
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
urine ultrasonography
veterinary virology
Record Number:   34230 
Unique Identifier:   D020159 

Occurrence in VHL:
 

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