Alkaptonuria is a rare metabolic disease leading to the accumulation of a blue-black pigment namely homogentisic acid in the cartilaginous tissue and body fluids giving them a black color. It is an autosomal recessive disease due to the deficiency of the hepatic enzyme oxidase which results in the accumulation of homogentisic acid in the skin, cartilage, and collagenous tissue giving them a black color. Herein we report a case of 65 years old gentleman who presented to our emergency department post domestic fall on his left hip, after which pain and swelling developed around the left hip and he was unable to bear weight with restricted mobility around the same
Background: Hip disease is a complication of Sickle Cell Disease most commonly occurs during adolesc...
WOS: 000355639400008PubMed ID: 25869213Introduction: Ochronotic arthropathy is a rapidly progressive...
Abstract Rapidly destructive osteoarthritis (RDO) of the hip is a rare condition characterized by ra...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria is a rare autosomal recessive disorder characterised by the absence of homogentisic aci...
A 56-year-old man presented to our orthopaedic clinic due to increasingly severe back pain. Physi-ca...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Background: Hip disease is a complication of Sickle Cell Disease most commonly occurs during adolesc...
WOS: 000355639400008PubMed ID: 25869213Introduction: Ochronotic arthropathy is a rapidly progressive...
Abstract Rapidly destructive osteoarthritis (RDO) of the hip is a rare condition characterized by ra...
Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that arises as a r...
Background: Ochronotic arthropathy is a rare complication in patients with alkaptonuria (AKU) that o...
AbstractINTRODUCTIONAlkaptonuria is an autosomal recessive disorder of metabolism. The pathogenesis ...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
Alkaptonuria, also called endogenous ochronosis, and also called as Black Urine Disease, is a rare m...
Introduction: Ochronosis is a metabolic disorder that is usually associated with the typical brown-b...
Alkaptonuria (AKU) is a rare disorder of autosomal recessive inheritance. It is caused by a mutation...
Alkaptonuria is a rare autosomal recessive disorder characterised by the absence of homogentisic aci...
A 56-year-old man presented to our orthopaedic clinic due to increasingly severe back pain. Physi-ca...
IntroductionAlkaptonuria is a rare autosomal recessive metabolic disorder which leads to accumulatio...
AbstractAlkaptonuria is a rare metabolic disease caused by a partial or total deficiency of homogent...
Alkaptonuria (AKU) or endogenous ochronosis is a very rare inborn error of tyrosine metabolism inher...
Background: Hip disease is a complication of Sickle Cell Disease most commonly occurs during adolesc...
WOS: 000355639400008PubMed ID: 25869213Introduction: Ochronotic arthropathy is a rapidly progressive...
Abstract Rapidly destructive osteoarthritis (RDO) of the hip is a rare condition characterized by ra...