-
Aminoaciduria occurs when the
urine contains abnormally high
amounts of
amino acids. In the
healthy kidney, the
glomeruli filter all
amino acids out of...
-
Dicarboxylic aminoaciduria is a rare form of
aminoaciduria (1:35 000 births)
which is an
autosomal recessive disorder of
urinary glutamate and aspartate...
-
Lysinuric protein intolerance Other names Hyperdibasic aminoaciduria type 2,Cationic
aminoaciduria or
Familial protein intolerance Lysine Specialty Endocrinology ...
- tryptophan) and
tryptophan in the
urine of
patients as part of a
generalized aminoaciduria of the disease. The
excessive loss of
tryptophan from malabsorption...
-
cystine stones in the kidneys, ureters, and bladder. It is a type of
aminoaciduria. "Cystine", not "cysteine," is
implicated in this disease; the former...
- cataracts, hypotonia,
intellectual disability,
proximal tubular acidosis,
aminoaciduria and low-molecular-weight proteinuria. Lowe
syndrome can be considered...
- >300 mg/d or >4 mg/kg per d with
normal levels blood/serum calcium)
Aminoaciduria (amino
acids in urine)
Phosphaturia (phosphate in urine) Glycosuria...
-
Fanconi syndrome, in
which there is also phosphaturia, glycosuria,
aminoaciduria, uricosuria, and
tubular proteinuria.[citation needed] The prin****l...
- and osteoporosis.
Renal tubular disease is
usually present causing aminoaciduria,
glycosuria and hypokalemia.
Cysteine deposition is most
evident in...
-
Metabolic and
nutritional diseases[citation needed]
Aminoaciduria or Lowe's
syndrome Cerebrotendineous xanthomatosis Diabetes mellitus Fabry's disease...
