Morgagni-Haenschen Syndrome

Morgagni–Haenschen syndrome: origin of the name, clinical picture, diagnostic approach, treatment and prognosis.

Morgagni-Henschen syndrome (Morgan syndrome; MHS) is a hereditary disease caused by mutations in the ESRP2 gene, which encodes matrix metalloprotease-9 (MMP-9), which has the ability to cut connector proteins between epithelial cells of the respiratory tract mucosa (