The two most familiar conditions associated with human FGF10 mutations are autosomal dominant aplasia of lacrimal and salivary glands (ALSG) (Entesarian et al., 2005; Seymen et al., 2017) and lacrimo-auriculo-dento-digital syndrome (LADD) (Milunsky et al., 2006; Rohmann et al., 2006), with both conditions lacking a primary lung complication. Here, FGF10 is linked to LADD syndrome.