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Master Gurkirat Grover, a 5-year-old male from Karnal, Haryana, has been diagnosed with argininosuccinate lyase deficiency, leading to multiple metabolic crises. His condition is managed through a low-protein diet, medications, and potential liver transplantation, which he recently underwent successfully with no complications. The disease is a rare genetic disorder affecting the urea cycle, and early diagnosis and multidisciplinary care are crucial for improving patient outcomes.

Author

Akanksha

Language

EN