Alkaptonuria is a genetic disorder characterized by an accumulation of homogentisic acid due to an enzymatic defec of homogentisate 1,2 dioxygenase. The homogentisic acid is excreted exclusively by both glomerular filtration and tubular secretion leading to the renal parenchyma being exposed to high concentrations of homogentisic acid. The alkaptonuric patients are at higher risk of renal stones (and of prostate stones for males), usually in the later stages of the disease. We describe the case of a 51-year-old man whose renal and prostate stones were analyzed by X-ray diffraction and infrared spectroscopy, respectively. We review the cases of alkaptonuria (AKU) patients reported in the literature for whomthe composition of kidney or prosta...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria (AKU) is a rare debilitating autosomal recessive disorder of tyrosine metabolism. Defic...
Background: Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the ac...
In alkaptonuria, the absence of homogentisic acid oxidase (HGO) results in the accumulation of homog...
The composition of a urinary tract stone often may be related to increased urinary concentration of ...
An elderly gentleman with chronic lower back and bilateral knee pain was found to have clinical and ...
Alkaptonuria (AKU) is a hereditary disorder that results from altered structure and function of homo...
Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the accumulation o...
The clinical effects of alkaptonuria (AKU) are delayed and ageing influences disease progression. Mo...
Alkaptonuria is a rare tyrosine metabolic disorder. A deficiency of homogentisic acid oxidase leads ...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Nephrolithiasis is one of the most frequent urologic diseases. The aim of this paper is to study the...
AbstractExtensive prostatic calculi in a young man should always elicit the suspicion of alkaptonuri...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria (AKU) is a rare debilitating autosomal recessive disorder of tyrosine metabolism. Defic...
Background: Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the ac...
In alkaptonuria, the absence of homogentisic acid oxidase (HGO) results in the accumulation of homog...
The composition of a urinary tract stone often may be related to increased urinary concentration of ...
An elderly gentleman with chronic lower back and bilateral knee pain was found to have clinical and ...
Alkaptonuria (AKU) is a hereditary disorder that results from altered structure and function of homo...
Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the accumulation o...
The clinical effects of alkaptonuria (AKU) are delayed and ageing influences disease progression. Mo...
Alkaptonuria is a rare tyrosine metabolic disorder. A deficiency of homogentisic acid oxidase leads ...
Two methods are described for homogentisic acid (HGA) determination in dried urine spots (DUS) on pa...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Nephrolithiasis is one of the most frequent urologic diseases. The aim of this paper is to study the...
AbstractExtensive prostatic calculi in a young man should always elicit the suspicion of alkaptonuri...
WOS: 000436882600003Aim: Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by ...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria (AKU) is a rare debilitating autosomal recessive disorder of tyrosine metabolism. Defic...
Background: Alkaptonuria, caused by a deficiency of homogentisate 1,2-dioxygenase, results in the ac...