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Kindler syndrome: Absence of definite ultrastructural feature

Kindler syndrome is characterized by congenital blister formation, photosensitivity, poikiloderma, and cutaneous atrophy in later life. There are few reports about the ultrastructural features of this syndrome, but still there is no consensus about the basic disease. Here we report a case of Kindler...

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Published in:	Journal of the American Academy of Dermatology 1999-02, Vol.40 (2), p.335-337
Main Authors:	Şentürk, Nilgün, Usubütün, Alp, Şahin, Sedef, Bükülmez, Gül, Erkek, Emel, Topaloğlu, Rezan, Akan, Tülin
Format:	Article
Language:	English
Subjects:	Basement Membrane - pathology Biological and medical sciences Biopsy Child Dermatology Epidermolysis Bullosa Dystrophica - genetics Epidermolysis Bullosa Dystrophica - pathology Female Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue Humans Medical sciences Rothmund-Thomson Syndrome - genetics Rothmund-Thomson Syndrome - pathology Skin - pathology Syndrome
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creator	Şentürk, Nilgün Usubütün, Alp Şahin, Sedef Bükülmez, Gül Erkek, Emel Topaloğlu, Rezan Akan, Tülin
description	Kindler syndrome is characterized by congenital blister formation, photosensitivity, poikiloderma, and cutaneous atrophy in later life. There are few reports about the ultrastructural features of this syndrome, but still there is no consensus about the basic disease. Here we report a case of Kindler syndrome with ultrastructural findings. (J Am Acad Dermatol 1999;40:335-7.)
doi_str_mv	10.1016/S0190-9622(99)70480-9
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subjects	Basement Membrane - pathology Biological and medical sciences Biopsy Child Dermatology Epidermolysis Bullosa Dystrophica - genetics Epidermolysis Bullosa Dystrophica - pathology Female Hereditary diseases of the skin. Congenital diseases of the skin. Haemangioma of the skin, of mucosae and of soft tissue Humans Medical sciences Rothmund-Thomson Syndrome - genetics Rothmund-Thomson Syndrome - pathology Skin - pathology Syndrome
title	Kindler syndrome: Absence of definite ultrastructural feature
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