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1.
An. bras. dermatol ; 92(2): 271-272, Mar.-Apr. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-838064

RESUMO

Abstract: Werner syndrome is a rare autosomal recessive disorder, caused by mutations in the WRN gene. Clinical findings include: senile appearance, short stature, grey hair, alopecia, bird-like face, scleroderma-like skin changes, skin ulcers, voice abnormalities, cataracts, osteoporosis, type 2 diabetes mellitus, ischemic heart disease and hypogonadism. The syndrome begins to become apparent in adolescence but it is usually diagnosed in the third or fourth decade of life. Since the patients usually die by the age of 40-50 years related to malignant neoplasms or atherosclerotic complications, they should be closely followed and treated for complications


Assuntos
Humanos , Masculino , Adulto , Síndrome de Werner/diagnóstico , Esclerodermia Localizada , Síndrome de Werner/complicações , Diagnóstico Diferencial , Úlcera da Perna/etiologia
2.
Indian J Dermatol Venereol Leprol ; 2016 May-June; 82(3): 313-314
Artigo em Inglês | IMSEAR | ID: sea-178203
3.
An. bras. dermatol ; 91(2): 156-159, Mar.-Apr. 2016. tab
Artigo em Inglês | LILACS | ID: lil-781366

RESUMO

Abstract BACKGROUND: Although the pathogenesis of androgenetic alopecia is not completely understood, the roles of genetic susceptibility and androgens are well-known. A lower ratio of the second digit (index finger = 2D) to the fourth digit (ring finger = 4D) length has been hypothesized to reflect prenatal androgen exposure and/or higher sensitivity to androgens. OBJECTIVES: To determine the relationship between the second to fourth digit length ratio and androgenetic alopecia. METHODS: Finger length measurements were made by a digital vernier calliper. Androgenetic alopecia severity was assessed using the Hamilton-Norwood scale. Subjects with an androgenetic alopecia score of grade III or more were included in the study. RESULTS: A total of 189 males with androgenetic alopecia and 171 healthy controls were enrolled in the study. The age range of participants was 19-65 years. The 2D:4D ratios in patients with androgenetic alopecia were significantly lower than those of healthy controls for the right hand; however, no significant difference was found for the left hand. Average 2D:4D ratios in androgenetic alopecia patients were also lower than in controls. No significant relationship was observed between androgenetic alopecia severity and 2D:4D ratios. CONCLUSION: Our data support the anatomical evidence of in utero androgen exposure and/or an individual’s sensitivity to androgens in patients with androgenetic alopecia. Furthermore, the right hand 2D:4D ratio might be an indicator of androgenetic alopecia development.


Assuntos
Humanos , Masculino , Feminino , Adulto , Idoso , Adulto Jovem , Efeitos Tardios da Exposição Pré-Natal/diagnóstico , Alopecia/diagnóstico , Dedos/anatomia & histologia , Tamanho do Órgão , Padrões de Referência , Valores de Referência , Índice de Gravidade de Doença , Gravidez , Marcadores Genéticos , Estudos de Casos e Controles , Antropometria/métodos , Valor Preditivo dos Testes , Reprodutibilidade dos Testes , Predisposição Genética para Doença , Alopecia/etiologia , Androgênios/análise , Androgênios/fisiologia
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