FGF10 and aplasia of lacrimal and salivary glands: Sequence alterations in the intracellular tyrosine-kinase domains of FGFR2 and FGFR3 were described to be involved in LADD syndrome [2,3], and aberrations of the FGF10 gene were found to be associated with both the ALSG and the LADD syndrome [2-6].