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Cystathioninuria - Wikipedia, the free encyclopedia
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Cystathioninuria , also called cystathionase deficiency , is an autosomal recessive metabolic disorder that results in an excess of cystathionine in the urine. It is associated with a congenital dy...
en.wikipedia.org/wiki/Cystathioninuria
MIM #219500 · Text · Description · Biochemical Features · Pathogenesis · Population Genetics · Molecular Genetics · See Also · References · Contributors ...
www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=219500
cystathioninuria /cys·ta·thi·o·nin·u·ria/ (sis″tah-thi″o-ne-nu´re-ah). 1. excess of cystathionine in the urine. 2. an inherited aminoacidopathy; ...
medical-dictionary.thefreedictionary.com/cystathioninur... medical-dictionary.thefreedictionary.com/cystathioninuria
A homogenate of liver obtained by biopsy from two patients with cystathioninuria, an inborn error of metabolism, cleaved radioactive cystathionine only ...
www.sciencemag.org/cgi/content/abstract/149/3688/1095
Psychology and Mental Health Dictionary Definitions - Cystathioninuria - Psychforums.com :
www.psychforums.com/definition/cystathioninuria.htm www.psychforums.com/definition/cystathioninuria.htm
Cystathioninuria was present in five of 11 patients with hepatoblastoma. Excretion ranged from68.8 to 7.2 mg in 24 hours, and from 597 to 72/~g/mg of ...
linkinghub.elsevier.com/retrieve/pii/S0022347680803337
Secondary cystathioninuria was found in two of 46 children suf- ... secondary cystathioninuria is uncommon in the diseases investigated. ...
www.springerlink.com/index/W810253354181037.pdf
Cystathioninuria symptoms, causes, diagnosis, and treatment information for Cystathioninuria (Gamma-cystathionase deficiency) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and prognosis. ... Cystathioninuria: Rare Disease...
www.wrongdiagnosis.com/medical/cystathioninuria.htm www.wrongdiagnosis.com/medical/cystathioninuria.htm
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www.ajcn.org/cgi/reprint/23/3/246
Studies of secondary cystathioninuria in three infants with untreated galactosemia are described. Excretion of cystathionine became normal and generalized aminoaciduria disappeared when galactose was eliminated from the diet.
pediatrics.aappublications.org/cgi/content/abstract/40/... pediatrics.aappublications.org/cgi/content/abstract/40/5/828