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erythrokeratodermia variabilis/retinoic acid

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NakalaMajaribio ya klinikiHati miliki
2 matokeo

[Erythrokeratodermia variabilis. Report of 3 clinical cases and evaluation of the topical retinoic acid treatment].

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Three cases of erythrokeratodermia variabilis are presented, the first one being a female aged 16 and the two others being a woman aged 27 and her son aged 2. Familial relationship between case 1 and the others did not exist. The inheritance pattern was apparently autosomal recessive in the first

Treatment of erythrokeratodermia variabilis with oral synthetic retinoids.

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
A thirty-one year old man and his ten year old daughter with the diagnosis of erythrokeratodermia variabilis, previously unresponsive to various topical agents and medication, were treated for seven weeks with oral retinoic acids. The response had been very good, particularly in the father. This is
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