LETTERS TO EDITOR: NETHERTON SYNDROME, A CASE REPORT AND REVIEW OF LITERATURE

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BOSKABADI HASSAN; MAAMOURI GHOLAMALI; MAFINEJAD SHAHIN

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Journal Paper

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Journal: Iranian Journal of Pediatrics Year:2013 | Volume:23 | Issue:5 Page(s): 611-612

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Information Journal Paper

Title

LETTERS TO EDITOR: NETHERTON SYNDROME, A CASE REPORT AND REVIEW OF LITERATURE

Author(s)

BOSKABADI HASSAN | MAAMOURI GHOLAMALI | MAFINEJAD SHAHIN | Issue Writer Certificate

Keywords

NETHERTON SYNDROME

FAILURE TO THRIVE

TRICHORHEXIS INVAGINATA

ERYTHRODERMA

Abstract

NETHERTON SYNDROME (NS) is a rare hereditary autosomal recessive multisystem disorder which presents with generalized ERYTHRODERMA at birth or soon after. Its incidence is estimated to be 1/200, 000. NS presents in most (but not all) patients with generalized ERYTHRODERMA and scaling resembling congenital ichthyosiform ERYTHRODERMA, or continuous peeling of the skin.Other common features of the disease are enteropathy, hypoalbuminemia, aminoaciduria, mental retardation, growth retardation, and immunologic abnormalities.

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APA: Copy

BOSKABADI, HASSAN, MAAMOURI, GHOLAMALI, & MAFINEJAD, SHAHIN. (2013). LETTERS TO EDITOR: NETHERTON SYNDROME, A CASE REPORT AND REVIEW OF LITERATURE. IRANIAN JOURNAL OF PEDIATRICS, 23(5), 611-612. SID. https://sid.ir/paper/669233/en

Vancouver: Copy

BOSKABADI HASSAN, MAAMOURI GHOLAMALI, MAFINEJAD SHAHIN. LETTERS TO EDITOR: NETHERTON SYNDROME, A CASE REPORT AND REVIEW OF LITERATURE. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2013;23(5):611-612. Available from: https://sid.ir/paper/669233/en

IEEE: Copy

HASSAN BOSKABADI, GHOLAMALI MAAMOURI, and SHAHIN MAFINEJAD, “LETTERS TO EDITOR: NETHERTON SYNDROME, A CASE REPORT AND REVIEW OF LITERATURE,” IRANIAN JOURNAL OF PEDIATRICS, vol. 23, no. 5, pp. 611–612, 2013, [Online]. Available: https://sid.ir/paper/669233/en

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