AbstractAlkaptonuria 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
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which causes o...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Alkaptonuria is a rare disorder of tyrosine catabolism. A 6 year old male child presented with histo...
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, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxida...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Aim:Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by a deficiency of homog...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Giriş: Alkaptonüri, tirozin metabolizmasıyla ilgili, karaciğerde bulunan bir enzim olan, homogentisa...
Alkaptonuria (AKU) is a multisystemic autosomal recessive disease due to deficiency of enzyme homoge...
Two patients with urinary findings suggestive of alcaptonuria were observed. One was a two-year-old ...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which causes o...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...
Alkaptonuria is a rare disorder of tyrosine catabolism. A 6 year old male child presented with histo...
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, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
Alkaptonuria is a rare disorder of metabolism characterized by deficiency of homogentisic acid oxida...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Aim:Alkaptonuria (AKU) is an autosomal recessively inherited disease caused by a deficiency of homog...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Giriş: Alkaptonüri, tirozin metabolizmasıyla ilgili, karaciğerde bulunan bir enzim olan, homogentisa...
Alkaptonuria (AKU) is a multisystemic autosomal recessive disease due to deficiency of enzyme homoge...
Two patients with urinary findings suggestive of alcaptonuria were observed. One was a two-year-old ...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Alkaptonuria is a rare autosomal recessive inherited disorder of tyrosine metabolism, which causes o...
This study aimed to determine the patient characteristics and clinical presentation of Alkaptonuria ...