Literature DB >> 4017274

Autoimmune polyendocrinopathy--candidosis--ectodermal dystrophy (APECED): autosomal recessive inheritance.

P Ahonen.   

Abstract

A genetic analysis was made of 58 patients and their 42 families with APECED (autoimmune polyendocrinopathy--candidosis--ectodermal dystrophy). APECED is characterized by hypoparathyroidism, primary adrenocortical failure and chronic mucocutaneous candidosis, but none of its components is constant. Other endocrine deficiencies can occur as well and also dystrophy of dental enamel and nails. The proportion of affected siblings was 0.147 +/- 0.034 (S.D.) when corrected for truncate single ascertainment, 0.246 +/- 0.019 when corrected for a priori truncate complete ascertainment and 0.240 +/- 0.047 when corrected for a posteriori truncate complete ascertainment. The male/female ratio was 1.04. The results are compatible with autosomal recessive transmission. No heterozygous manifestations of the gene were found. The gene is enriched in isolated subpopulations in central and eastern Finland. APECED is part of the "Finnish heritage of disease".

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Year:  1985        PMID: 4017274     DOI: 10.1111/j.1399-0004.1985.tb02037.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  32 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

Review 2.  Mechanisms of self-nonself discrimination and possible clinical relevance.

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3.  Management of squamous cell cancer of the oesophagus in a patient with a polyglandular endocrinopathy (APECED) and achalasia.

Authors:  Orla Mc Cormack; Marie Timlin; Anne Mc Gowan; Marie-Louise Healy; Narayanasamy Ravi; John V Reynolds
Journal:  J Gastrointest Surg       Date:  2012-04-05       Impact factor: 3.452

Review 4.  Update on Aire and thymic negative selection.

Authors:  Geraldo A Passos; Cesar A Speck-Hernandez; Amanda F Assis; Daniella A Mendes-da-Cruz
Journal:  Immunology       Date:  2017-09-26       Impact factor: 7.397

5.  Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.

Authors:  C Ding; B Buckingham; M A Levine
Journal:  J Clin Invest       Date:  2001-10       Impact factor: 14.808

6.  Regulation of insulin gene expression by cytokines and cell-cell interactions in mouse medullary thymic epithelial cells.

Authors:  D Levi; C Polychronakos
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Review 7.  Central tolerance to self revealed by the autoimmune regulator.

Authors:  Alice Y Chan; Mark S Anderson
Journal:  Ann N Y Acad Sci       Date:  2015-11       Impact factor: 5.691

8.  Chronic active hepatitis in the type I polyglandular autoimmune syndrome.

Authors:  T M Michele; J Fleckenstein; A R Sgrignoli; P J Thuluvath
Journal:  Postgrad Med J       Date:  1994-02       Impact factor: 2.401

9.  A common and recurrent 13-bp deletion in the autoimmune regulator gene in British kindreds with autoimmune polyendocrinopathy type 1.

Authors:  S H Pearce; T Cheetham; H Imrie; B Vaidya; N D Barnes; R W Bilous; D Carr; K Meeran; N J Shaw; C S Smith; A D Toft; G Williams; P Kendall-Taylor
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

10.  Reversible hyperkinesia in a patient with autoimmune polyglandular syndrome type I.

Authors:  T Baumert; G Kleber; J Schwarz; A Stäbler; R Lamerz; K Mann
Journal:  Clin Investig       Date:  1993-11
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