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SAM syndrome which is characterized by severe dermatitis, multiple allergies and metabolic wasting is a congenital skin disease caused by mutations in the genes encoding either desmoglein-1 or desmoplakin.
Available treatments targeting th17 cells incluide biologic drugs that are currently licensed for psoriasis therapy. Such as ustekinumab and secukinumab. Ustekinumab was recently evaluated in two patients with DSP mutations but we had obtained littlecutaneous improvement in another patient with SAM syndrome who had DSG1 mutations.
If traeted early, meconial aspiration syndrome has a positive prognosis and does not have to present further complications.
Between 9 and 15% of the participants are complicated by the presence of meconium in amniotic fluid and historically 5 to 12% of those cases developed SAM. This figure has dropped in developed countries to percentages between 1.6 to 3.9%.
The major effect of secukinumab in ours patients quality of life supports interleukin-17A as a new target to treat patients with serious skin disorders
Treg would also join this group of cells that act both collaboratively and regulatoryly, since in addition to their known suppressive function they would also coordinate the first steps of viral infection directly as well as indirectly inducing, by secreting TGF- the diferrentiation of TH17.