Congenital Ichthyosis: A Case Treated Successfully With Acitretin

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Congenital Ichthyosis: A Case Treated Successfully With Acitretin

INTRODUCTION Lamellar ichthyosis (collodion baby) is a cornification disorder classified under the category of autosomal recessive congenital ichthyosis and characterized by hyperkeratosis. Early-stage retinoid treatment has been shown to improve survival in these patients. In this article, a lamellar ichthyosis case is presented of an infant who had the symptoms at birth and was treated succes...

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Treatment Of Congenital Ichthyosis With Acitretin

We assessed the clinical efficacy, tolerability and safety of acitretin in a patient with ichthyosis. A newborn infant with ichthyosis who presented at birth with collodion baby appearance, was treated with acitretin. A moderate response to acitretin therapy (1 mg/kg/day) administered for 6 months was observed, with improvement in cutaneous lesions. Clinical improvement was achieved shortly aft...

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Psoriasis is a chronic inflammatory skin disease that involves immune-mediated cutaneous inflammation and keratinocyte hyperproliferation. Psoriasis in patients with HIV responds poorly to treatment and has a high morbidity rate, thus posing a challenge to clinicians. Until now, there have been no documented cases of acitretin therapy for HIV-associated psoriasis in Korea. Here, we report a cas...

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Report of a Congenital Ichthyosis

A case of congenital ichthiosis 1s presented. Histo­logic pattern and the treatment is discussed. 

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A case of harlequin ichthyosis treated with isotretinoin.

Harlequin ichthyosis is a rare congenital ichthyosis classified under the category of Autosomal Recessive Congenital Ichthyoses, which also include lamellar ichthyosis and congenital ichthyosiform erythroderma. It is caused by functional null mutations in the ABCA12 gene, a keratinocyte lipid transporter associated with lamellar granule formation. Patients have a classic clinical presentation a...

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ژورنال

عنوان ژورنال: Iranian Journal of Pediatrics

سال: 2016

ISSN: 2008-2142,2008-2150

DOI: 10.5812/ijp.2442