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1.
J Cutan Aesthet Surg ; 14(3): 374-376, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34908786

RESUMO

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.
Artigo em Inglês | MEDLINE | ID: mdl-25593795

RESUMO

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.
Artigo em Inglês | MEDLINE | ID: mdl-23716806
4.
Indian J Dermatol ; 57(5): 335-42, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23112351

RESUMO

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.
Artigo em Inglês | MEDLINE | ID: mdl-20534088

RESUMO

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.


Assuntos
Catepsina C/genética , Doença de Papillon-Lefevre/genética , Mutação Puntual , Adulto , Alelos , Éxons/genética , Humanos , Masculino , Doença de Papillon-Lefevre/diagnóstico por imagem , Doença de Papillon-Lefevre/patologia , Radiografia
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