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Tyrosinemia Type 3: Causes, Symptoms, Diagnosis, and Management

Tyrosinemia is a rare genetic metabolic disorder in which the body cannot break certain building blocks of proteins. Read the article to know more about it.

Dr. Shakshi Jain

28 Jun 2023 . 4 min read

Tyrosinemia Type II: Causes, Symptoms, and Treatment

Tyrosinemia type II is a genetic condition characterized by high blood levels of the amino acid tyrosine that affect the skin, eyes, and intellectual growth.

Hemamalini. R

06 May 2024 . 5 min read

Nitisinone - Indications, Contraindications, Adverse Effects, Dosage, Warnings, and Precautions.

Nitisinone is used to treat hereditary tyrosinemia type 1 (HT-1). Read the article to learn more.

Dr. Vincy Infantina

13 Mar 2024 . 9 min read

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Disclaimer: All health articles published on this website are not intended to be a substitute for professional medical diagnosis, advice or treatment by a trained physician. Seek the advice from your physician or other qualified health-care providers with questions you may have regarding your symptoms and medical condition for a complete medical diagnosis. Do not delay or disregard seeking professional medical advice because of something you have read on this website. 



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