Literature DB >> 2594954

Candidiasis-endocrinopathy syndrome with progressive myopathy.

R A Evans1, J N Carter, B Shenston, A Smith, E Hills, R Walls, A Corbett.   

Abstract

A women suffering from the candidiasis-endocrinopathy syndrome, developed severe myopathy in her fourth decade and died from it at the age of 37 years. Associated conditions were hypoparathyroidism, vitiligo, chronic mucocutaneous candidiasis, short stature, intellectual disability, ovarian failure and alopecia totalis. Muscle biopsy findings were non-specific with focal atrophy of type 2 fibres. Serum immunoglobulin levels were normal. The only demonstrable abnormalities of her immune system were impaired T-cell function and antibody production by B-cells (detectable to smooth muscle, mitochondria and gastric parietal cells). The T-cell abnormality may have been part of a more generalized cell defect, resulting from an unidentified genetic abnormality, whilst the circulating antibodies could have been a response to tissue damage. There was no convincing evidence of primary autoimmune damage.

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Mesh:

Year:  1989        PMID: 2594954

Source DB:  PubMed          Journal:  Q J Med        ISSN: 0033-5622


  2 in total

1.  French-Canadian families from Saguenay-Lac-Saint-Jean: a new founder population for APECED.

Authors:  Tania Cruz Marino; Hélène Villeneuve; Josianne Leblanc; Caroline Duranceau; Philippe Caron; Charles Morin; Marcel Milot; Raphaëlle Chrétien; Maude-Marie Gagnon; Jean Mathieu; Benjamin Ellezam; Daniela Buhas
Journal:  Endocrine       Date:  2021-11-30       Impact factor: 3.633

2.  Thoracic aortic calcification in 3 children with candidiasis-endocrinopathy syndrome.

Authors:  A Shikata; T Sugimoto; K Kosaka; T Tehara; S O Kido; H Matsuo; T Sawada; W E Berdon; H G Herrod; L Parvey
Journal:  Pediatr Radiol       Date:  1993
  2 in total

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