Zusammenfassung
Beschreibung von je drei Kindern mit idiopathischem M. Addison in zwei Familien, die als Kusins zweiten Grades miteinander verwandt sind. Literaturübersicht der bekannten familiären Fälle von primär chronischidiopathischer Nebennierenrindeninsuffizienz. Genetische Analyse des uns bekannten Materials. In der Mehrzahl der Fälle scheint der Erbgang autosomal-recessiv zu sein.
Summary
Description of six children in two families (three in each) with idiopathic Addisons disease, related as second cousins. Information about published familial cases of chronic idiopathic insufficiency of adrenal glands. In most of the cases heredity seems to be of the autosomalerecessive type.
Literatur
Anderson, J. R., R. B. Goudie, G. C. Gray, and G. C. Timbury: Auto-antibodies in Addison's disease. Lancet 1957/I, 1123.
Andrewes, F. W.: Two cases of tuberculosis with unusual pigmentation of the skin and deposit in the suprarenals. St. Bart. Hosp. Rep. 27, 109 (1891).
Bamatter, F.: Hypocorticisme primitif. Cours d'endocrinologie infantile, Genève 1958 (Ed. Centre internat. Enfance, Paris 1959).
Battistini, A., e F. Carmine: Il Morbo di Addison nel bambino. Lattante 34, 109 (1963).
Baumann, Th.: Funktion und Erkrankung der Nebenniere im Kindesalter. Dtsch. Ges. inn. Med. 50, 178 (1938).
Berlin, R.: Addison's disease: familial incidence and occurence in association with pernicious anemia. Acta med. scand. 144, 1 (1952).
Bie, J.: Morbus Addisonii hos børn (Addison's disease in 2 siblings). Nord. Med. 55, 193 (1956).
Blizzard, R. M., R. W. Chandler, M. A. Kyle, and W. Hung: Adrenal antibodies in Addison's disease. Lancet 1962/II, 901.
Borghini, G.: Morbo di Addison familiare. G. Clin. med. 18, 1435 (1937).
Boyd, J. F., and A. M. Macdonald: Adrenocortical hypoplasia in siblings. Arch. Dis. Childh. 35, 561 (1960).
Briggs, J. N., J. F. Goodwin, and A. Wilson: Addison's disease occurring in two brothers. Brit. med. J. 1951/I, 115.
Brøchner-Mortensen, K.: Familial occurrence of Addison's disease. Acta med. scand. 156, 205 (1956).
de Cock, J., J. de Graeff, D. Smeenk u. A. Querido: Chronische primaire bijnierinsufficientie. Ned. T. Geneesk. 101, 2426 (1957).
Craig, J. M., L. H. Schiff, and J. E. Boone: Chronic moniliasis associated with Addison's disease. Amer. J. Dis. Child. 89, 669 (1955).
Croom, D. H.: Addisonism as a family disease. Lancet 1909/I, 603.
Curschmann, H.: Über familiären Morbus Addison und Addisonismus. Wien. med. Wschr. 90, 327 (1940).
Dhom, G.: Die Nebennierenrinde im Kindesalter. Berlin-Heidelberg-New York: Springer 1965.
Fahr, T., u. F. Reiche: Zur Frage des Morbus Addison. Frankfurt. Z. Path. 22, 231 (1919).
Fanconi, A., A. Prader, W. Isler, F. Luethy u. R. Siebenmann: Morbus Addison mit Hirnsklerose im Kindesalter. Ein hereditäres Syndrom mit X-chromosomaler Vererbung? Helv. paediat. Acta 18, 480 (1963).
Felber, J. P.: Détermination de l'ACTH par une méthode radioimmunologique. Sympos. radioakt. Isotope, Bad Gastein 1964.
Fleming, R. A., and J. Miller: A family with Addison's disease. Brit. med. J. 1900/I, 1014.
Fournier, P.: La maladie d'Addison chez l'enfant (à propos de 5 observations compartant 2 cas familiaux). Thèse (Lyon) 253 (1960).
Gagnon, J., et R. Leblanc: Sclérose cérébrale diffuse avec mélanodermie et atrophie surrénale. Un. méd. Can. 88, 392 (1959).
Gambaro, C.: Iposurrenalismo familiare. Pediat. int. (Roma) 12, 335 (1962).
de Gennes, L., H. Bricaire et L. Moreau: Les insuffisances surrénales infracliniques ou frustes. Presse méd. 67, 619 (1959).
di George, A. M., and K. Paschkis: The syndrome of Addison's disease, hypoparathyroidism an superficial moniliasis. Amer. J. Dis. Child. 94, 476 (1957).
Gittler, R. D., S. S. Fajans, and J. W. Conn: Coexistance of Addison's disease and diabetes mellitus. J. clin. Endocr. 19, 797 (1959).
Harris-Jones, J. N., and P. G. F. Nixon: Familial Addison's disease with spastic paraplegia. J. clin. Endocr. 15, 739 (1955).
Hewitt, P. H.: Addison's disease occurring in sisters. Brit. med. J. 1957/II, 1530.
Hiekkala, H.: Idiopathic hypoparathyroidism, adrenal insufficiency and moniliasis in children. Ann. Pediat. Fenn. 10, 213 (1964).
Hung, W., C. J. Migeon, and R. H. Parrott: A possible autoimmune basis for Addison's disease in three siblings, one with idiopathic hypopara-thyreoidism, pernicious anemia and superficial moniliasis. New Engl. J. Med. 269, 658 (1963).
Jaudon, J. C.: Addison's disease in children. J. Pediat. 28, 737 (1946).
Koegel, R., J. de Haller, F. Bamatter et A. F. Muller: Maladie d'Addison familiale. Helv. paediat. Acta (im Druck).
Labhart, A.: Klinik der inneren Sekretion, S. 302 ff. Berlin-Göttingen-Heidelberg: Springer 1957.
Lewin, G.: Über den Morbus Addison. Charité-Ann. 17, 536 (1892).
Meakin, J. W., D. H. Nelson, and C. W. Thorn: Addison's disease in two brothers. J. clin. Endocr. 19, 726 (1959).
Mitchell, R. G., and K. Rhaney: Congenital adrenal hypoplasia in siblings. Lancet 1959/I, 488.
Mitchell, R. G., and K. Rhaney: Congenital adrenal hypoplasia. Lancet 1963/II, 1065.
Moehlig, R. C.: Addison's disease followed for nine years: case report with autopsy. J. clin. Endocr. 7, 134 (1947).
Morabito, F.: Sul morbo di Addison e le sue forme fruste nell'infanzia. Pediatria (Napoli) 35, 969 (1927).
Mosier, H. D.: Hypoplasia of the pituitary and adrenal cortex. J. Pediat. 48, 633 (1956).
Mozziconacci, P., J. L'Hirondel, F. Girard et C. Attal: Maladie d'Addison familiale avec insuffisance surrenale dissociée. Sem. Hôp. Paris 36, 1529 (1960).
Neumann, J.: Zur Addison'schen Krankheit. Münch med. Wschr. 63 488 (1916).
Quinto, M. G., S. L. Leikin, and W. Hung: Pernicious anemia in a young girl associated with idiopathic hypoparathyreoidism, familial Addison's disease and moniliasis. J. Pediat. 64, 241 (1964).
Patzer, T.: Wrodzona hipplazza hadnerczy u niemowlat do lat. Pediat. pol. 39, 327 (1964).
Penman, R. W. B.: Addison's disease in association with spastic paraplegia. Brit. Med. J. 1960/I, 402.
Prader, A., G. J. P. A. Anders u. M. Habich: Zur Genetik des kongenitalen, adrenogenitalen Syndroms. Helv. paediat. Acta 17, 271 (1962).
Roselli, A., and L. T. Barbosa: Congenital hypoplasia of the adrenal glands. Report of two cases in sisters with necropsy. Pediatrics 35, 70 (1965).
Royer, P., H. Lestradet, C. H. de Menibus et G. Vermeil: Hypoaldostéronisme familial chronique à début néonatal. Sem. Hôp. Paris 37, 901 (1961).
Schwab, L. W.: Addison's disease, two cases in one family. J. Amer. med. Ass. 30, 708 (1898).
Shepard, T. H., B. H. Landing, and D. G. Mason: Familial Addison's disease. Amer. J. Dis. Child. 97, 154 (1959).
Smith, M. E., J. Cough, and O. P. Galpin: Addison's disease in identical twins. Brit. Med. J. 1963/II, 1316.
Smith, T. W., and A. R. Higgins: Addison's disease in two brother with serum hepatitis in one. Milit. Surg. 110, 180 (1952).
Stempfel, R. S., and F. L. Engel: A congenital, familial syndrome of adrenocortical insufficiency without hypoaldosteronism. J. Pediat. 57, 443 (1960).
Sunder, J. H., J. V. Bonessi, W. R. Balash, and T. S. Danowski: Addison's disease in relation to diabetes mellitus. New Engl. J. Med. 272, 818 (1965).
Sutphin, A., F. Albright, and D. J. Maccune: Five cases (three in siblings) of idiopathic hypoparathyroidism associated with moniliasis. J. clin. Endocr. 3, 625 (1943).
Symonds, C. P.: Familial incidence of Addison's disease. Brit. med. J. 1958/I, 100.
Talbot, N. B., E. H. Sobel, J. W. Macarthur, and J. D. Crawford: Functional endocrinology from birth to adolescence. Cambridge (Mass.) Harvard University Press 1952.
Toccafondi, R., e A. Borghi: Morbo di Addison familiare (Iposurrenalismo cronico “parzialmente compensato” insoste in padre e figlio dopo l'influenza asiatica). Acta Genet. med. (Roma) 11, 407 (1962).
Turpin, R., J. Lafourcade, R. Gorin, B. Caille, J. Terris, A. Defranoux, C. Salama et G. Normand L'atrophie corticosurrénale de l'enfant. Sem. Hôp. Paris 37, 2123 (1961).
Wakefield, E. G., and E. E. Smith: Addison's disease, suprarenalopathies, sclerosis of the glands of internal secretion. Amer. J. med. Sci. 174, 343 (1927).
Welch, R. G.: Addison's disease in a nine year old girl. Brit. med. J. 1957/I, 980.
Whitaker, J., B. H. Landing, V. M. Esselborn, and R. R. Williams: The syndrome of familial juvenile hypoadrenocorticism, hypoparathyreoidism and superficial moniliasis. J. clin. Endocr. 16, 1374 (1956).
Williams, A., and M. J. Robinson: Addison's disease in infancy. Arch. Dis. Childh. 31, 265 (1956).
Williams, H. E., and M. Freeman: Primary familial Addison's disease. Aust. paediat. J. 1, 93 (1965).
Wolff, S.: Female pseudohermaphroditism with adrenocortical failure in identical twins. Arch. Dis. Childh. 29, 132 (1954).
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Nöthiger, F. Familiärer Morbus Addison. Z. Kinder-Heilk. 99, 14–32 (1967). https://doi.org/10.1007/BF00517818
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DOI: https://doi.org/10.1007/BF00517818