Polyglandular autoimmune syndrome type I with ano-genital condylomata acuminata, mucocutaneous candidiasis, vitiligo, corneal lesion and primary hypoparathyroidism;Genito-anale condylomata acuminata, mukokutane candidose, vitiligo, keratopathie und primarer hypoparathyreoidismus bei autoimmunem polyglandularem syndrom typ 1

Deutsche Medizinische Wochenschrift

Volumn 122, Issue 45, 1997, Pages 1382-1386

  Oblinger, E ^a   Cibis, A ^b   Peter, R U ^a   Proebstle, T M ^c  

^a UNIVERSITY OF ULM   (Germany)

^b Abteilung Dermatologie der Universität   (Germany)

^c BUNDESWEHRKRANKENHAUS ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOTRANSFERASE; AMPHOTERICIN B; CALCITRIOL; GLUCONATE CALCIUM; LACTIC ACID; LIVER ENZYME; PARATHYROID HORMONE;

ADULT; ARTICLE; AUTOIMMUNITY; CASE REPORT; CAUTERIZATION; CLONAL ANERGY; CONDYLOMA ACUMINATUM; CORNEA DISEASE; FEMALE; HEPATITIS; HUMAN; HYPOPARATHYROIDISM; MUCOCUTANEOUS CANDIDIASIS; SYNDROME; VITILIGO;

EID: 0030782014     PISSN: 00120472     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1047775     Document Type: Article

References (12)

1. Aaltonen, J., P. Björses, L Sandkuijl, J. Perheentupa. L. Peltonen. An autosomal locus causing autoimmune disease. Autoimmune polyglandular disease type I assigned to chromosome 21. Nature Genetics 8 (1994), 83-87.
2. Ahonen, P.. Autoimmune polyendocrinopathy candidosis-ectodermal dystrophy (APECED). Autosomal recessive inheritance. Clin. Genet. 27 (1985). 535-542.
3. Ahonen, P., S. Myllärniemi, I. Sipila.J. Perheentupa. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in series of 68 patients. New Engl. J. Med. 322 (1990), 1829-1836.
4. Arulanantham, K., J. M Kwyer, M. Genel. Evidence for defective immunoregulation in the syndrome of familial candidiasis endocrinopathy. New Engl. J. Med. 300 (1979), 164-168.
5. Krohn. K., R. Uibo, E. Aavik, P. Peterson, K. Savilahti. Identification by molecular cloning of an autoantigen associated with Addison's disease as steroid 17-a-hydroxytase. Lancet 339 (1992), 770-773.
6. Kunin. A. S., B. R. MacKay, S. L Burns., M. J. Halberstam. The syndrome of hypoparathyroidism and adrenocortical insufficiency, a possile sequel of hepatitis. Case report and review of the literature. Amer. J. Med. 34 (1963), 856-866.
7. Neufeld, M., N. MacLaren, R. Blizzard. Autoimmune polyglandular syndrome. Pediat. Ann. 9 (1980), 154-162.
8. Neufeld, M., N. MacLaren, R. Blizzard. Two types of autoimmune Addison's disease associated with different polyglandular autoimmune (PGA) syndromes. Medicine 60 (1981 ), 355-362.
9. Perheentupa, J.. Autoimmune polyendocrinopathy-candidosisectodermal dystrophy (APECED). In Eriksson A. W., H. R. Forsius, H. R. Nevanlinna, P. L Workman, R. K. Norio. Population Structure and Genetic Disorders (Academic Press. New York 1980), 583-587.
10. Saenger, P., L S. Lebine, W. J. Irvine, K. Gottesdiener, W. Rauh, N. Sonino, D. Chow, M. I. New. Progressive adrenal failure in polyglandular autoimmune disease. J. clin. Endocrinol. Metabol. 54 (1982), 863-868.
11. Tsai, R.J., S. C. G.Tseng. Human allograft limbal transplantation for cornea surface reconstruction. Cornea 13 (1994), 389-400.
12. Zlotogora, J., S. M. Shapiro. Polyglandular autoimmune syndrome type I among IrianianJews.J. Med. Genet. 29 (1992). 824-826.