Endogenous ochronosis/Alkaptonuria is a rare, genetic metabolic disease presenting with cutaneous hyperpigmentation, disabling arthropathy, and homogentisic aciduria. The dermoscopic features of this entity have a good correlation with the histopathological findings, and its knowledge can facilitate early diagnosis to decrease long-term morbidity and improve the quality of life
Brief reportOchronosis is a rare disease characterised clinically by bluish-grey skin discolouration...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
Ochronosis or alkaptonuria is a rare, autosomal recessive metabolic disease where the enzyme homogen...
Endogenous ochronosis (EO) or alkaptonuria is an inherited autosomal recessive disease caused by the...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Alkaptonuria is a rare, autosomal-recessive disorder of phenylalanine/tyrosine metabolism due to con...
Ochronosis is a rare disease characterized by speckled and diffuse pigmentation symmetrically over t...
Ochronosis (alkaptonuria) is an autosomal recessive inherited metabolic disease that causes pigmenta...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Alkaptonüri, nadir görülen otozomal resesif geçişli bir doğumsal metabolizma hastalığıdır. Tirozin v...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
The formally accepted meaning of the term ochronosis is musculoskeletal and skin manifestation of al...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
Brief reportOchronosis is a rare disease characterised clinically by bluish-grey skin discolouration...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
Ochronosis or alkaptonuria is a rare, autosomal recessive metabolic disease where the enzyme homogen...
Endogenous ochronosis (EO) or alkaptonuria is an inherited autosomal recessive disease caused by the...
Endogenous ochronosis or alkaptonuria is a rare, autosomal recessive disease of tyrosine metabolism ...
Abstract: Alkaptonuria, also called endogenous ochronosis, is a rare metabolic autosomal recessive d...
Alkaptonuria is a rare, autosomal-recessive disorder of phenylalanine/tyrosine metabolism due to con...
Ochronosis is a rare disease characterized by speckled and diffuse pigmentation symmetrically over t...
Ochronosis (alkaptonuria) is an autosomal recessive inherited metabolic disease that causes pigmenta...
Alkaptonuria, a rare disorder of amino acid metabolism, is characterised by the excretion in the uri...
Alkaptonüri, nadir görülen otozomal resesif geçişli bir doğumsal metabolizma hastalığıdır. Tirozin v...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
The formally accepted meaning of the term ochronosis is musculoskeletal and skin manifestation of al...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
Brief reportOchronosis is a rare disease characterised clinically by bluish-grey skin discolouration...
Ochronosis is a cutaneous disorder caused by the accumulation of phenols, either endogenously as hom...
Ochronosis or alkaptonuria is a rare, autosomal recessive metabolic disease where the enzyme homogen...