Final answer:
The given information describes the condition of galactosemia.
Step-by-step explanation:
Galactosemia is an inherited disorder that affects the body's ability to process galactose, a sugar found in lactose. The deficiency of G1p-uridyl-transferase enzyme impairs the breakdown of galactose, leading to its accumulation and subsequent damage to various organs.
When someone with galactosemia consumes lactose, the body is unable to convert galactose into glucose, which is the usable form of sugar. As a result, galactose builds up in the body and can cause damage to various organs.
The accumulation of galactose can lead to problems such as liver damage, kidney problems, cataracts, and intellectual disabilities. In infants, galactosemia can cause failure to thrive, poor feeding, and jaundice.
To manage galactosemia, individuals need to follow a strict galactose-free diet, avoiding foods that contain lactose or galactose. This means avoiding dairy products, as well as foods that contain milk, whey, lactose, or galactose.
If galactosemia is not properly managed, it can lead to serious health complications. Therefore, early diagnosis and adherence to the recommended diet are crucial for individuals with this disorder.
Your question is incomplete, but most probably the full question was:
•Deficient G1p-uridyl- transferase.
• G1p accum to damage kidney, liver, brain.
• Sxs = MR direct hyperbili & jaundice, ↓glc, cataracts, seizures.
• Predisposed to E. coli sepsis.
• No lactose por vida.
Q: The given information is about a condition involving of what ?