Polyradiculoneuropathy indicative of wiskott syndrome - Aldrich on a case

Wiskott-Aldrich syndrome (WAS) is a rare inherited immune deficiency of recessive transmission linked to the X chromosome, manifested by hemorrhagic signs, eczema and whose hematological study shows severe thrombocytopenia. Cellular and humoral responses, which are triggered during infection can lead to the development of neuropathies