RIT1 p.Thr83Pro variant is associated with severe neonatal outcomes in Noonan syndrome cases
RIT1 Variant Linked to Severe Cases of Noonan Syndrome
This case report and literature review examines the RIT1 c.247A>C (p.Thr83Pro) variant in neonates with Noonan syndrome. The authors identif…
A specific genetic variant in the RIT1 gene is linked to severe, life-threatening complications in infants with Noonan syndrome.
Case report describes secukinumab use in a woman with erythrodermic psoriasis and systemic capillary leak syndrome
One case report links secukinumab to severe capillary leak syndrome in a woman with psoriasis
This case report details the clinical course of a 66-year-old woman with new-onset erythrodermic psoriasis who developed systemic capillary …
A woman with psoriasis developed life-threatening capillary leak syndrome after starting secukinumab, with symptoms improving only after sto…