Hypomelanosis of Ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10),+13/46,XY]
dc.authorid | Yakıncı, Mehmet Cengiz/0000-0001-5930-4269 | |
dc.authorid | DURMAZ, YASAR/0000-0002-4437-0068 | |
dc.authorid | Kutlu, Nurettin Onur/0000-0002-3306-6570 | |
dc.authorwosid | Yakıncı, Mehmet Cengiz/ABI-7519-2020 | |
dc.authorwosid | DURMAZ, YASAR/JVO-4824-2024 | |
dc.authorwosid | Kutlu, Nurettin Onur/AAW-6196-2021 | |
dc.contributor.author | Yakinci, C | |
dc.contributor.author | Kutlu, NO | |
dc.contributor.author | Alp, MN | |
dc.contributor.author | Senol, M | |
dc.contributor.author | Durmaz, Y | |
dc.contributor.author | Budak, T | |
dc.date.accessioned | 2024-08-04T20:58:58Z | |
dc.date.available | 2024-08-04T20:58:58Z | |
dc.date.issued | 2002 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | The term hypomelanosis of Ito (HI) has been used as a diagnosis for individuals with swirly hypopigmentation or depigmentation distributed along the lines of Blaschko. HI should be appropriately evaluated for a possible association with chromosomal or genetic mosaicism or chimerism. We report a six-month-old severely motor and mental retarded boy with these typical cutaneous lesions associated with extracutaneous features, including facial dysmorphism, polydactyly, and inguinal. hernia. The cytogenetic examination of lymphocytes kdemonstrated a mosaicism of 46, XY, der (13;13) (q10;q10), +13/46, XY. This is the first case reported in the literature showing an association between phylloid pigmentary pattern of hypomelanosis of Ito and trisomy 13 mosaicism. | en_US |
dc.identifier.endpage | 155 | en_US |
dc.identifier.issn | 0041-4301 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 12026206 | en_US |
dc.identifier.startpage | 152 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/103335 | |
dc.identifier.volume | 44 | en_US |
dc.identifier.wos | WOS:000175316000013 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Turkish J Pediatrics | en_US |
dc.relation.ispartof | Turkish Journal of Pediatrics | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | hypomelanosis of Ito | en_US |
dc.subject | trisomy 13 mosaicism | en_US |
dc.subject | phylloid cutaneous pattern | en_US |
dc.subject | West's syndrome | en_US |
dc.title | Hypomelanosis of Ito with trisomy 13 mosaicism [46, XY, der (13;13) (q10;q10),+13/46,XY] | en_US |
dc.type | Article | en_US |