Background: Type 1 congenital plasminogen deficiency (hypoplasminogenaemia) is a rare
autosomal recessive congenital condition caused by mutations in the plasminogen gene …

Type 1 plasminogen deficiency is a rare genetic disorder. Type 1 plasminogen deficiency is
characterized by fibrin-rich pseudomembrane formation on mucosal surfaces, particularly …

C-PLGD is a rare autosomal recessive multisystem disorder of the fibrinolytic system.
Mutations in the PLG gene result in extravascular fibrinous deposits, termed ligneous for …

Congenital plasminogen deficiency is a rare disorder associated with extravascular
formation of fibrin-rich ligneous pseudomembranes on mucosal surfaces caused by a variety …

A Successful Treatment Approach in 2 Patients With Type 1 Pl... : Journal of Pediatric
Hematology/Oncology A Successful Treatment Approach in 2 Patients With Type 1 Plasminogen …

Plasminogen deficiency type 1 (PLGD-1, hypoplasminogenemia) is an ultra-rare, lifelong
disease associated with development of fibrinous lesions in multiple organ systems …

Ligneous conjunctivitis is a rare and unusual form of chronic pseudomembranous
conjunctivitis which usually starts in early infancy. Plasminogen deficiency has recently been …

Discussion Plasminogen deficiency is a rare entity that affects 1.6 of every 1 million
individuals and is inherited in an autosomal recessive manner by mutations in homozygosis …

Type 1 congenital plasminogen deficiency (CPD) is a rare autosomal recessive disease
which causes formation of fibrin pseudomembranes that affect multiple systems/organs: the …

Congenital plasminogen deficiency is an extremely rare autosomal recessive disorder that
leads to formation of extravascular fibrin rich pseudomembranes in various organ systems …