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DOI: 10.1111/j.1365-2133.1986.tb02829.x
OpenAccess: Closed
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Pachyonychia congenita Jackson-Lawler type: a distinct malformation syndrome

Maurizio Clementi,Edda Cardin de Stefani,Camillo Dei Rossi,V. Avventi,Romano Tenconi

Hyperhidrosis
Dermatology
Hyperkeratosis
1986
A family with three members in two generations affected by pachyonychia congenita, hyperkeratosis and hyperhidrosis of the palms and soles, follicular keratosis, neonatal teeth and epidermoid cysts (Jackson‐Lawler syndrome) is described. The nosological autonomy of this condition is proposed and a further heterogeneity is suggested on the basis of histopathological changes in the subcutaneous cysts.
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    Pachyonychia congenita Jackson-Lawler type: a distinct malformation syndrome” is a paper by Maurizio Clementi Edda Cardin de Stefani Camillo Dei Rossi V. Avventi Romano Tenconi published in 1986. It has an Open Access status of “closed”. You can read and download a PDF Full Text of this paper here.