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ANE syndrome
rareANE syndrome is a rare, genetic, neuro-endocrino-cutaneous disorder characterized by highly variable degrees of alopecia, moderate to severe intellectual disability, progressive, late-onset motor deterioration and combined anterior pituitary hormone deficiency, manifesting with central hypogonadotropic hypogonadism, delayed or absent puberty, growth hormone deficiency (resulting in short stature), progressive central adrenal insufficiency and a hypoplastic anterior pituitary gland. Additional features include hypodontia, flexural reticulate hyperpigmentation, gynecomastia, microcephaly and kyphoscoliosis.
- Identifiers
- MONDO:0012794 OMIM:612079Orphanet:157954
- Causal genes
- RBM28
- Part of
- Congenital hypogonadotropic hypogonadismIntegumentary system disorderNon-acquired combined pituitary hormone deficiencySyndromic disease
- Also known as
- alopecia, neurologic defects, and endocrinopathy syndrome · alopecia-progressive neurological defect-endocrinopathy syndrome · anes
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