The authors describe two brothers showing leukonychia totalis in association with deafness, hyperkeratosis palmaris and plantaris, scalp modifications and dental lesions. The onychopathia began during early childhood and was also present in four other members of the same family. All nails of both hands and feet were affected and appeared white, dull and with inconspicuous lunulae. The hair was rough, dark, bristly, looking like steel wire. In particular, the changes of the hair shaft were studied under scanning electron microscope. Hair dysplasia, accompanied by structural changes such as complete and incomplete twistings, longitudinal grooves and modified imbrication, was found. After briefly reviewing the literature on the subject, the authors point out the suggestive hypothesis that all these manifestations might possibly we ascribed to a single genetic defect, in spite of their different clinical features in the various patients.

Leukonychia totalis and ectodermal dysplasia. Report of 2 cases / C.Crosti, F.Sala, E. Bertani, G.Gasparini, S.Menni. - In: ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE. - ISSN 0151-9638. - 110:8(1983), pp. 617-622.

Leukonychia totalis and ectodermal dysplasia. Report of 2 cases

C. Crosti
Primo
;
S. Menni
Ultimo
1983

Abstract

The authors describe two brothers showing leukonychia totalis in association with deafness, hyperkeratosis palmaris and plantaris, scalp modifications and dental lesions. The onychopathia began during early childhood and was also present in four other members of the same family. All nails of both hands and feet were affected and appeared white, dull and with inconspicuous lunulae. The hair was rough, dark, bristly, looking like steel wire. In particular, the changes of the hair shaft were studied under scanning electron microscope. Hair dysplasia, accompanied by structural changes such as complete and incomplete twistings, longitudinal grooves and modified imbrication, was found. After briefly reviewing the literature on the subject, the authors point out the suggestive hypothesis that all these manifestations might possibly we ascribed to a single genetic defect, in spite of their different clinical features in the various patients.
Settore MED/35 - Malattie Cutanee e Veneree
1983
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/189942
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