Tracheobronchomegaly (Mounier-Kuhn syndrome) and Bronchiectasis as rare manifestations of Homocystinuria

Homocystinuria (HCU) is a rare autosomal recessive inherited disorder usually diagnosed in childhood. It is characterized by a deficiency of the enzyme that converts homocysteine to cystathionine. The accumulation of homocysteine leads to abnormalities in the ocular, skeletal, cardiovascular, and ce...

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Bibliographic Details

Published in:	Respiratory Medicine Case Reports
Main Authors:	Aasir M. Suliman, Mohamed A. Alamin, Maha M. Hamza
Format:	Article
Language:	English
Published:	Elsevier 2023-01-01
Subjects:	Homocystinuria Bronchiectasis Tracheobronchomegaly Mounier-Kuhn syndrome Fibrillin degeneration
Online Access:	http://www.sciencedirect.com/science/article/pii/S2213007123000035