We report on two sisters affected by congenital alopecia, nail dystrophy, and a severe T-cell immunodeficiency, presumably inherited as an autosomal-recessive disorder. The T-cell defect was characterized by severe functional impairment, as shown by the lack of proliferative response and upregulation of activation markers following mitogen stimulation. The functional abnormality occurred in spite of the presence of phenotypically mature of the defect. This is the first observation reported on an ectodermal disorder, characterized by alopecia and nail dystrophy, observed at birth, in association with a primary immunodeficiency. The hypothesis that these two events may be casually related is discussed.

Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two siblings / Pignata, Claudio; Castaldo, A.; Sebastio, G. F.; Porta, F.; Guarino, Alfredo. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. - ISSN 0148-7299. - ELETTRONICO. - 65:(1996), pp. 167-170.

Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two siblings.

PIGNATA, CLAUDIO;GUARINO, ALFREDO
1996

Abstract

We report on two sisters affected by congenital alopecia, nail dystrophy, and a severe T-cell immunodeficiency, presumably inherited as an autosomal-recessive disorder. The T-cell defect was characterized by severe functional impairment, as shown by the lack of proliferative response and upregulation of activation markers following mitogen stimulation. The functional abnormality occurred in spite of the presence of phenotypically mature of the defect. This is the first observation reported on an ectodermal disorder, characterized by alopecia and nail dystrophy, observed at birth, in association with a primary immunodeficiency. The hypothesis that these two events may be casually related is discussed.
1996
Congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two siblings / Pignata, Claudio; Castaldo, A.; Sebastio, G. F.; Porta, F.; Guarino, Alfredo. - In: AMERICAN JOURNAL OF MEDICAL GENETICS. - ISSN 0148-7299. - ELETTRONICO. - 65:(1996), pp. 167-170.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/155926
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