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Linear and whorled naevoid hypermelanosis: a case with systemic involvement and trisomy 18 mosaicism

✍ Scribed by M. Komine; M. Hino; M. Shiina; I. Kanazawa; Y. Soma; K. Tamaki


Book ID
104460007
Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
65 KB
Volume
146
Category
Article
ISSN
0007-0963

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πŸ“œ SIMILAR VOLUMES


Further case of trisomy 18 mosaicism wit
✍ Collins, A. L. ;Fisher, J. ;Crolla, J. A. ;Cockwell, A. E. πŸ“‚ Article πŸ“… 1995 πŸ› John Wiley and Sons 🌐 English βš– 185 KB πŸ‘ 2 views

this journal published a case report of trisomy 18 mosaicism in a 13-year-old girl with normal intelligence, delayed pubertal development, and growth failure [Sarigol and Rogers, 19941. We now report a further case of trisomy 18 mosaicism with a mild phenotype, this time presenting with congenital a

Hypomelanosis of Itoβ€”a nonspecific marke
✍ Chitayat, David ;Friedman, J. M. ;Johnston, Margaret M. πŸ“‚ Article πŸ“… 1990 πŸ› John Wiley and Sons 🌐 English βš– 333 KB πŸ‘ 2 views

We report on a patient with hypomelanosis of Ito (HI), developmental delay, recurrent pneumonia, and facial asymmetry. Chromosome analysis done on blood and on one of three skin biopsies showed trisomy 18 mosaicism. This is the first report of HI associated with trisomy 18 mosaicism. This neuroectod