Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report

Author:

Ponti Giovanni,Pellacani Giovanni,Tomasi Aldo,Percesepe Antonio,Guarneri Carmelo,Guerra Azzurra,Mandel Victor Desmond,Kisla Elif,Cevikel Piril,Neri Claudia,Menozzi Cristina,Seidenari Stefania

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Reference24 articles.

1. Ito M: Studies on melanin. Tohoku J Exp Med. 1952, 55: 1-104. 10.1620/tjem.55.Supplement_1.

2. Ronger S, Till M, Kanitakis J, Balme B, Thomas L: Hypomelanosis of Ito in a girl with Trisomy 13 mosaicism: a cytogenetic study. Ann Dermatol Venereol. 2003, 130: 1033-1038.

3. Vormittag W, Ensinger C, Raff M: Cytogenetic and dermatoglyphic findings in a familial case of Hypomelanosis of Ito (incontinentia pigmenti achromians). Clin Genet. 1992, 41: 309-314.

4. Ruggieri M, Pavone L: Hypomelanosis of Ito: clinical syndrome or just phenotype?. J Child Neurol. 2000, 15: 635-644. 10.1177/088307380001501001.

5. Flannery DB, Byrd JR, Freeman WE, Perlman SA: Hypomelanosis of Ito: a cutaneous marker of chromosomal masaicism. Am J Hum Genet. 1985, 37: A93-

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1. Unilateral Syndactyly, Hemihypertrophy, and Hyperpigmentation with Mosaic 2q35 Deletion;Indian Journal of Dermatology;2023-09

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3. Hypomelanosis of Ito (Incontinentia Pigmenti Achromians);Neurocutaneous Disorders;2022

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