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Publikováno v:
International Journal of Biomedical and Advance Research. 5:131
Kindler syndrome is a very rare hereditary disorder characterized by acral blister formation in infancy and childhood, progressive poikiloderma, cutaneous atrophy and increased photosensitivity. Since it was first described by Kindler in 1954, less t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03624b4f8002a8c2154c000b961c2728
https://doi.org/10.7439/ijbar.v5i2.650
https://doi.org/10.7439/ijbar.v5i2.650
