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Neuroectodermal-endocrine syndrome

rare

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.

Identifiers
MONDO:0017045 Orphanet:2676
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPolyendocrinopathy
Also known as
neuroectodermal endocrine syndrome · Oerter-Friedman-Anderson syndrome

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