Alkaptonuria is a rare disorder of tyrosine catabolism. A 6 year old male child presented with history of darkish staining of the toilet commode following voiding. The urine when kept in a sterile container for a few hours turned black. Urine examination showed massive amounts of homogentisic acid. Patient was diagnosed as alkaptonuria
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the accumulation o...
In alkaptonuria, the absence of homogentisic acid oxidase (HGO) results in the accumulation of homog...
AbstractAlkaptonuria is a rare disorder of tyrosine catabolism. A 6 year old male child presented wi...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxid...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxida...
Alkaptonuria is a rare, autosomal-recessive disorder of phenylalanine/tyrosine metabolism due to con...
Alkaptonuria is an extremely rare condition, which is due to a defect in protein metabolism. The mos...
Alkaptonuria (AKU) is a multisystemic autosomal recessive disease due to deficiency of enzyme homoge...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Alkaptonuria, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
Alkaptonuria caused by compound heterozygote mutations: Alkaptonuria is a rare autosomal recessive d...
Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the accumulation o...
In alkaptonuria, the absence of homogentisic acid oxidase (HGO) results in the accumulation of homog...
AbstractAlkaptonuria is a rare disorder of tyrosine catabolism. A 6 year old male child presented wi...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxid...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxida...
Alkaptonuria is a rare, autosomal-recessive disorder of phenylalanine/tyrosine metabolism due to con...
Alkaptonuria is an extremely rare condition, which is due to a defect in protein metabolism. The mos...
Alkaptonuria (AKU) is a multisystemic autosomal recessive disease due to deficiency of enzyme homoge...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Alkaptonuria, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
Alkaptonuria caused by compound heterozygote mutations: Alkaptonuria is a rare autosomal recessive d...
Alkaptonuria (ALK) is a rare genetic disorder, characterized by binding of ochronotic pigment to the...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the accumulation o...
In alkaptonuria, the absence of homogentisic acid oxidase (HGO) results in the accumulation of homog...
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