NETHERTON SYNDROME: REPORT OF TWO CASES

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AKHIANI M.; KIAVASH K.; KAMYAB KAMBIZ; SEYRAFI H.

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Journal Paper

Paper Information

Journal: Iranian Journal of Dermatology Year:2008 | Volume:10 | Issue:4 (42) Page(s): 353-358

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Information Journal Paper

Title

NETHERTON SYNDROME: REPORT OF TWO CASES

Author(s)

AKHIANI M. | KIAVASH K. | KAMYAB KAMBIZ | SEYRAFI H. | Issue Writer Certificate

Keywords

NETHERTON SYNDROMEQ3

GENODERMATOSISQ3

ERYTHRODEMAQ3

TRICHORRHEXIS INVAGINATAQ3

ICHTHYOSIS LINEARIS CIRCUMFLEXAQ3

Abstract

NETHERTON SYNDROME is a rare autosomal recessive condition with variable expression. It comprises an ichthyosiform dermatitis and erythroderma of variable intensity associated with hair abnormalities and features of atopy. The pathognomic (required for diagnosis) feature is TRICHORRHEXIS INVAGINATA identified by microscopic examination of hair shaft. ICHTHYOSIS LINEARIS CIRCUMFLEXA is another typical lesion that may not always be observed. It comprises an episodic migrating erythematous and scaling annular and polycyclic flat patch with an advancing double edge of peeling scale. Here we present two cases of NETHERTON SYNDROME with characteristic manifestations mentioned above.

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APA: Copy

AKHIANI, M., KIAVASH, K., KAMYAB, KAMBIZ, & SEYRAFI, H.. (2008). NETHERTON SYNDROME: REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY, 10(4 (42)), 353-358. SID. https://sid.ir/paper/57780/en

Vancouver: Copy

AKHIANI M., KIAVASH K., KAMYAB KAMBIZ, SEYRAFI H.. NETHERTON SYNDROME: REPORT OF TWO CASES. IRANIAN JOURNAL OF DERMATOLOGY[Internet]. 2008;10(4 (42)):353-358. Available from: https://sid.ir/paper/57780/en

IEEE: Copy

M. AKHIANI, K. KIAVASH, KAMBIZ KAMYAB, and H. SEYRAFI, “NETHERTON SYNDROME: REPORT OF TWO CASES,” IRANIAN JOURNAL OF DERMATOLOGY, vol. 10, no. 4 (42), pp. 353–358, 2008, [Online]. Available: https://sid.ir/paper/57780/en

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