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erythrokeratodermia variabilis/retinoic acid

Sábháiltear an nasc chuig an gearrthaisce
AiltTrialacha cliniciúlaPaitinní
2 torthaí

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

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
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.

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
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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Clóscríobh symptom nó galar agus léigh faoi luibheanna a d’fhéadfadh cabhrú, luibh a chlóscríobh agus galair agus comharthaí a úsáidtear ina choinne a fheiceáil.
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