HARLEQUIN ICHTHYOSIS: A REPORT OF TWO CASES

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OMID A.; KATEBI M.; GHANNAD KAFI SH.; JAFARIAN AMIR HOSSEIN; TAVASSOLIAN H.

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Journal Paper

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Journal: Iranian Journal of Dermatology Year:2005 | Volume:8 | Issue:2 Page(s): 149-154

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Information Journal Paper

Title

HARLEQUIN ICHTHYOSIS: A REPORT OF TWO CASES

Author(s)

Keywords

HARLEQUINQ4

ICHTHYOSISQ4

CONGENITAL ICHTHYOSISQ3

Abstract

HARLEQUIN ICHTHYOSIS is one of the most severe congenital skin cornification disorders with an incidence rate of about I in 300,000 births and characteristic clinical features. We report two cases of HARLEQUIN ICHTHYOSIS (HI) or HARLEQUIN fetus (HF), which were products of consanguineous union. Clinical examination showed typical features of HARLEQUIN ICHTHYOSIS, with the presence of plaques with diamond-like configuration, external ear anomaly, severe ectropion and eclabium, and rigid semi flexion of limbs.

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APA: Copy

OMID, A., KATEBI, M., GHANNAD KAFI, SH., JAFARIAN, AMIR HOSSEIN, & TAVASSOLIAN, H.. (2005). HARLEQUIN ICHTHYOSIS: A REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY, 8(2), 149-154. SID. https://sid.ir/paper/57916/en

Vancouver: Copy

OMID A., KATEBI M., GHANNAD KAFI SH., JAFARIAN AMIR HOSSEIN, TAVASSOLIAN H.. HARLEQUIN ICHTHYOSIS: A REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2005;8(2):149-154. Available from: https://sid.ir/paper/57916/en

IEEE: Copy

A. OMID, M. KATEBI, SH. GHANNAD KAFI, AMIR HOSSEIN JAFARIAN, and H. TAVASSOLIAN, “HARLEQUIN ICHTHYOSIS: A REPORT OF TWO CASES,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 8, no. 2, pp. 149–154, 2005, [Online]. Available: https://sid.ir/paper/57916/en

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