Alkaptonuria: Introduction, Symptoms, Causes, Lab Diagnosis, and Treatment
Table of Contents
Alkaptonuria is an enzyme deficiency, homogentisic dioxygenase (HGD) rare inherited disorder. It is used to break down a toxic substance called homogentisic acid. Excess of homogentisic acid causes bones and cartilage to become discolored and brittle which causes later osteoarthritis, especially in the spine and large joints. The patient who has this condition also has urine that turns dark brown or black when it is exposed to air (as shown in the above image).
The following are the common symptoms of Alkaptonuria-
There is no specific treatment so far. Rather, treatment is focused mainly on managing symptoms.
Introduction An anemometer measures wind speed. It also measures wind pressure. The name comes from…
Introduction TB-LAMP (Tuberculosis Loop-Mediated Isothermal Amplification) is a manual, rapid molecular diagnostic test endorsed by…
Introduction The NALC-NaOH (N-acetyl-L-cysteine–sodium hydroxide) method is the gold standard for processing clinical specimens in…
Introduction The BD BACTEC™ MGIT™ 960 (Mycobacteria Growth Indicator Tube) is a fully automated, high-volume…
Introduction Trichosporon is a genus of anamorphic, yeast-like basidiomycetous fungi widely distributed in nature, particularly…
Introduction Saprochaete capitata is an emerging opportunistic fungal pathogen that causes severe, frequently fatal systemic…
View Comments
I am not rattling wonderful with English but I get hold this really easy to read .