A Rare Case of Methionine Adenosyltransferase Deficiency in an 8-Month-Old Infant Presenting with Jaundice and Bleeding Episodes

Authors

  • Mohammad Yunus Choudhary

Keywords:

Abstract

Methionine adenosyltransferase MAT deficiency is a rare inherited disorder of methionine metabolism that can lead to a wide range of symptoms including jaundice bleeding episodes and neurological impairment We report the case of an 8-month-old female infant who presented with yellowish discoloration of skin distended abdomen and bleeding episodes On further evaluation she was found to have high levels of methionine in her blood A diagnosis of MAT deficiency was made and was started on appropriate treatment with a methioninerestricted diet and supplements

How to Cite

Mohammad Yunus Choudhary. (2023). A Rare Case of Methionine Adenosyltransferase Deficiency in an 8-Month-Old Infant Presenting with Jaundice and Bleeding Episodes. Global Journal of Medical Research, 23(F6), 37–37. Retrieved from https://medicalresearchjournal.org/index.php/GJMR/article/view/102406

A Rare Case of Methionine Adenosyltransferase Deficiency in an 8-Month-Old Infant Presenting with Jaundice and Bleeding Episodes

Published

2023-08-07