Neuroectodermal-endocrine syndrome

MONDO:0017045

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.

Also known as: Oerter-Friedman-Anderson syndrome, neuroectodermal endocrine syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Neuroectodermal-endocrine syndrome itself.

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↑ Polyendocrinopathy (81) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Neuroectodermal-endocrine syndrome (0)

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