Hartnup's Disease || Tryptophan Metabolic Disorder || NEET PG || Biochemistry
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4 سال پیش
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This the video on HARTNUP'S
This the video on HARTNUP'S DISEASE with NEET PG and AIIMS mcqs.
It is an Inherited disorder of tryptophan metabolism.
This disorder was first of all reported in the family of Hartnup
Defect in the intestinal and renal transport of tryptophan and other neutral amino acids and leads to tryptophan deficiency.
Tryptophan deficiency leads to decreased synthesis of vitamin niacin and serotonin.
Decreased synthesis of niacin leads to pellagra like symptoms and decreased serotonin synthesis is responsible for neurological symptoms
It is an Inherited disorder of tryptophan metabolism.
This disorder was first of all reported in the family of Hartnup
Defect in the intestinal and renal transport of tryptophan and other neutral amino acids and leads to tryptophan deficiency.
Tryptophan deficiency leads to decreased synthesis of vitamin niacin and serotonin.
Decreased synthesis of niacin leads to pellagra like symptoms and decreased serotonin synthesis is responsible for neurological symptoms
4 سال پیش
در تاریخ 1398/12/28 منتشر شده
است.
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