Format

Send to

Choose Destination
See comment in PubMed Commons below
Dermatol Online J. 2014 Feb 18;20(2). pii: doj_21540.

A case of harlequin ichthyosis treated with isotretinoin.

Author information

1
Kaiser Permanente Los Angeles Medical Center. laura.mos.chang@gmail.com.

Abstract

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 at delivery and need neonatal intensive care treatment to maximize their chances of survival. Early oral retinoid therapy has been shown to increase survival in patients with harlequin ichthyosis, and we present a case of a 9-month-old male with this condition who has been treated with isotretinoin since day 7 of life.

PMID:
24612573
[Indexed for MEDLINE]
Free full text
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Arthur C Huntley MD, California Digital Library
    Loading ...
    Support Center