Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Familial candidiasis 1 is an autosomal dominant disorder caused by genetic alterationsin the cytogenetic region 2p22.3-p21 which may be accompanied by thyroid disease.
Familial candidiasis
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CLEC6A
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Familial candidiasis 2
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Familial candidiasis 3
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Familial candidiasis 4
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Familial candidiasis 5
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Familial candidiasis 6
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Familial candidiasis 8
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Familial candidiasis 9
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| 1. |
Sams WM et al. (1979) Chronic mucocutaneous candidiasis. Immunologic studies of three generations of a single family. 
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| 2. |
Canales L et al. (1969) Immunological observations in chronic mucocutaneous candidiasis.
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| 3. |
Wells RS et al. (1972) Familial chronic muco-cutaneous candidiasis.
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| 4. |
Montes LF et al. (1971) Prolonged oral treatment of chronic mucocutaneous candidiasis with Amphotericin B.
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| 5. |
Jorizzo JL et al. (1980) Cimetidine as an immunomodulator: chronic mucocutaneous candidiasis as a model.
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| 6. |
Zimmermann-Belsing T et al. (1994) Riedel's thyroiditis: an autoimmune or primary fibrotic disease?
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| 7. |
Loeys BL et al. (1999) Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis.
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| 8. |
Atkinson TP et al. (2001) An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single family.
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| 9. |
Zuccarello D et al. (2002) Familial chronic nail candidiasis with ICAM-1 deficiency: a new form of chronic mucocutaneous candidiasis.
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| 10. |
Ee HL et al. (2005) Autosomal dominant familial chronic mucocutaneous candidiasis associated with acne rosacea.
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