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1.
J Cutan Aesthet Surg ; 14(3): 374-376, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34908786

RESUMEN

We report a 39-year-old man who presented with skin-colored plaque over the glabella and root of the nose. Histopathology revealed the diagnosis of trichoblastoma. This case is reported to emphasize the rare presentation of trichoblastoma as it usually presents as an isolated nodule.

2.
Indian Dermatol Online J ; 5(Suppl 2): S104-5, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25593795

RESUMEN

Targeted ultraviolet B phototherapy is used in the treatment for localized variants of psoriasis. We present two cases in which we compared the efficacy of lite spot and lite brush in the treatment of psoriasis and vitiligo.

3.
Indian J Dermatol ; 58(2): 146, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23716806
4.
Indian J Dermatol ; 57(5): 335-42, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23112351

RESUMEN

Photoprotection by sunscreens, clothing and glasses are important to protect the skin against the detrimental effects of sun exposure. In order to achieve complete protection, topical strategies must shield against the range of solar wavelengths ultraviolet A, ultraviolet B, infrared radiation that can damage the skin. To provide the necessary broad spectrum coverage, combinations of chemical and physical UV filters along with molecules that are capable of interfering with and/or preventing the deleterious effects of sunlight are discussed in this review.

5.
Int J Dermatol ; 49(5): 541-3, 2010 May.
Artículo en Inglés | MEDLINE | ID: mdl-20534088

RESUMEN

Papillon-Lefevre syndrome and Haim Munk syndrome are palmoplantar keratodermas associated with premature periodontal destruction. The additional findings of Haim Munk Syndrome include onychogryphosis, arachnodactyly, acral osteolysis and pes planus. Both are associated with mutations in the lysosomal protease cathepsin C. We describe a patient with phenotype for Haim Munk Syndrome and genetic analysis revealed a homozygous point mutation in exon 1 of the gene encoding cathepsin C.


Asunto(s)
Catepsina C/genética , Enfermedad de Papillon-Lefevre/genética , Mutación Puntual , Adulto , Alelos , Exones/genética , Humanos , Masculino , Enfermedad de Papillon-Lefevre/diagnóstico por imagen , Enfermedad de Papillon-Lefevre/patología , Radiografía
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