Williams-Campbell Syndrome

Williams-Campbell syndrome (WCS) is a congenital disorder which was first described in 1960 by Howard Williams and Peter Campbell among five children with respiratory manifestations due to cartilage deficiency of the bronchial walls (Williams and Campbell 1960). The first case of familial WCS in siblings was described in 1976 (Wayne and Taussig 1976). The prevalence of WCS is not yet determined because it is so rare. Also, the time of onset is usually during childhood (Rohilla et al. 2021).