Immunodeficiency due to ficolin 3 deficiency

Common Name(s)

Immunodeficiency due to ficolin 3 deficiency

Individuals with ficolin-3 deficiency have highly variable manifestations and a variable age of symptom onset. Some patients may show increased susceptibility to infection in the perinatal or neonatal period, whereas others may show autoimmune features as adults. Ficolin-3, also known as H-ficolin, can activate the lectin pathway of the complement system; deficiency may thus lead to defects in the complement system (summary by {3:Munthe-Fog et al., 2009} and {1:Michalski et al., 2015}). For a discussion of genetic heterogeneity of lectin complement activation pathway defects, see LCAPD1 ({614372}).
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Immunodeficiency due to ficolin 3 deficiency" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

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Symptoms, Diagnosis, and Treatment

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Clinical Trial Information This information is provided by ClinicalTrials.gov

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