Other Syndromes with Prominent Ectodermal Dysplasia Signs
摘要
ED are divided in major groups of diseases using molecular pathways: EDA1 pathway, WNT pathway, TP63 pathway or in functional-structural pathways (cadherins, nectins, keratins-related ED). Rare complex syndromes with specific ectodermal derivative abnormalities recently reported (i.e., ALPK1-related autoinflammatory syndrome) are listed separately in this chapter.