Retinohepatoendocrinologic syndrome is characterized by total colorblindness caused by progressive cone dystrophy, degenerative liver disease, and endocrine dysfunction (hypothyroidism, diabetes, repeated abortions or infertility). It has been described in six females from two sibships with a high degree of consanguinity, and in a male from another family.
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Bangstad syndrome
MONDO:0008874
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
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autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome
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multiple polyglandular tumor
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neuroectodermal-endocrine syndrome
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autoimmune polyendocrinopathy
MONDO:0017278