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1.
Iranian Journal of Dermatology. 2007; 9 (4): 361-366
Dans Anglais | IMEMR | ID: emr-83150

Résumé

The Proteus syndrome comprises an association of asymmetrical overgrowth of almost any part of the body, verrucous epidermal naevi, vascular malformations and lipoma-like subcutaneous hamartoma. Both sexes are affected with equal frequency and severity and it is not transmitted genetically. Here a 16-year-old man with asymmetric overgrowth of the extremities, macrodactyly, cerebriform hypertrophy of the soles and various skin and bony lesions is reported diagnosed as Proteus syndrome


Sujets)
Humains , Mâle , Malformations multiples , Anomalies morphologiques congénitales des membres , Hamartomes
2.
Iranian Journal of Dermatology. 2005; 8 (2): 145-148
Dans Persan | IMEMR | ID: emr-71253

Résumé

Mal de Meleda [keratoderma palmoplantaris transgrediens] is a rare autosomal recessive form of palmoplantar keratoderma with hyperkeratosis of palms and soles, which appears soon after birth and progressively involves other areas [transgrediens] of the skin especially dorsal aspects of hands and feet. We report a 20-year-old woman with Mal de Meleda with some unusual clinical features, i.e. peculiar finger nail anomalies and pseudoainhum on all her fingers


Sujets)
Humains , Femelle , Kératose palmoplantaire/étiologie , Kératose palmoplantaire/génétique , Hyperkératose épidermolytique , Ongles malformés
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