Neuroectodermal-endocrine syndrome is characterized by a combination of endocrine and neuroectodermal abnormalities, including low growth hormone levels, delayed puberty, type II diabetes mellitus, mild intellectual deficit, sensorineural deafness, characteristic facial appearance and alopecia. It has been described in four sibs from Myanmar. The disease is neuroectodermal-endocrine syndrome (MONDO_0017045). Also known as: Oerter-Friedman-Anderson syndrome.