Abstract
ADDISON disease or adrenal insufficiency is usually acquired, but genetic forms have been recognised. Hyperpigmentation and hypoglycaemia are the major manifestations.
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References
Addison T (1849) Anaemia: Disease of the supra-renal capsules. London Hosp Gaz 43: 517–518
Fanconi A, Prader A, Isler W, Luthy F, Siebenmann RE (1964) Morbus Addison mit Hirnsklerose im Kindesalter. Ein hereditaeres Syndrom mit X-chromo-somaler Vererbung? Helv Paediatr Acta 18: 480–501
Martin MM (1971) Familial Addison’s disease. Birth Defects Original Article Series VII(6): 98–100
Phair JP, Bondy PK, Abelson DM (1965) Diabetes mellitus, Addison’s disease and myxoedema: report of two cases. J Clin Endocr 25: 260–265
Shepard TH, Landing BH, Mason DG (1959) Familial Addison’s disease. Case reports of two sisters with corticoid deficiency unassociated with hypoal-dosteronism. Am J Dis Child 97:154–162
Sutherland FM (1960) Nova et Vetera. Thomas Addison 1793–1860. Br Med J 5194: 304–305
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© 1997 Springer-Verlag London Limited
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Beighton, P., Beighton, G. (1997). ADDISON, Thomas. In: The Person Behind the Syndrome. Springer, London. https://doi.org/10.1007/978-1-4471-0925-9_1
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DOI: https://doi.org/10.1007/978-1-4471-0925-9_1
Publisher Name: Springer, London
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