KINDLER SYNDROME AND EPIDERMOLYSIS BULLOSA SIMPLEX, REPORT OF THREE CASES

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SEYRAFI H.; FARNAGHI F.; GHANINIEZHAD H.

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Journal Paper

Paper Information

Journal: TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ) Year:2000 | Volume:58 | Issue:1 Page(s): 104-108

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Information Journal Paper

Title

KINDLER SYNDROME AND EPIDERMOLYSIS BULLOSA SIMPLEX, REPORT OF THREE CASES

Author(s)

SEYRAFI H. | FARNAGHI F. | GHANINIEZHAD H. | Issue Writer Certificate

Keywords

KINDLER SYNDROMEQ4

EPIDERMOLYSIS BULLOSA SIMPLEXQ4

WEARY- KINDLER SYNDROMEQ4

Abstract

KINDLER SYNDROME is characterize by acral blister formation in infancy and childhood, poikiloderma and cutaneous atrophy. Undoubtedly, similarities of the clinical features exist between KINDLER SYNDROME and EPIDERMOLYSIS BULLOSA SIMPLEX with mottled pigmentation. In this article, we report three patients with KINDLER SYNDROME. Until the bullous component of KINDLER SYNDROME is more completely understood, we believe that this disorder should continue to be classified as a sperate disease.

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APA: Copy

SEYRAFI, H., FARNAGHI, F., & GHANINIEZHAD, H.. (2000). KINDLER SYNDROME AND EPIDERMOLYSIS BULLOSA SIMPLEX, REPORT OF THREE CASES. TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), 58(1), 104-108. SID. https://sid.ir/paper/38120/en

Vancouver: Copy

SEYRAFI H., FARNAGHI F., GHANINIEZHAD H.. KINDLER SYNDROME AND EPIDERMOLYSIS BULLOSA SIMPLEX, REPORT OF THREE CASES. TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ)[Internet]. 2000;58(1):104-108. Available from: https://sid.ir/paper/38120/en

IEEE: Copy

H. SEYRAFI, F. FARNAGHI, and H. GHANINIEZHAD, “KINDLER SYNDROME AND EPIDERMOLYSIS BULLOSA SIMPLEX, REPORT OF THREE CASES,” TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), vol. 58, no. 1, pp. 104–108, 2000, [Online]. Available: https://sid.ir/paper/38120/en

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