author = {Khatu, Swapna. and More, Yuvraj. and Vankawala, Divyank. and Chavan, Deepali. and Gokhale, Neeta.}, title = {{Alkaptonuria: Case report}}, journal ={Medical Journal of Dr. D.Y. Patil University}, volume ={8}, number ={1}, pages = {84-86}, doi = {10.4103/0975-2870.148860}, year = {2015}, abstract ={Alkaptonuria is a rare, autosomal-recessive disorder of phenylalanine/tyrosine metabolism due to congenital deficiency of the enzyme homogentisic acid oxidase. Herein, we are reporting a classical case of alkaptonuria with extensive skin pigmentation and skeletal involvement. Histopathological examination also revealed classical ochre-colored deposits in dermis.}, URL ={https://journals.lww.com/mjdy/pages/default.aspx/article.asp?issn=0975-2870;year=2015;volume=8;issue=1;spage=84;epage=86;aulast=Khatu;t=6}, eprint ={https://journals.lww.com/mjdy/pages/default.aspx/article.asp?issn=0975-2870;year=2015;volume=8;issue=1;spage=84;epage=86;aulast=Khatu;t=6} }