New Association Between Ring Chromosome 20 Syndrome and Hypomelanosis of Ito
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,Neurology,Pediatrics, Perinatology and Child Health
Reference19 articles.
1. Heterogeneous seizure manifestations in hypomelanosis of Ito: Report of four new cases and review of the literature;Assogba;Neurol Sci,2010
2. Studies of melanin: XI. Incontinentia pigmenti achromians: A singular case of nevus depigmentosus systematicus bilateralis;Ito;Tohoku J Exp Med,1952
3. Hypomelanosis of Ito: Neurological complications in 34 cases;Pascual-Castroviejo;Can J Neurol Sci,1988
4. Hypomelanosis of Ito: No entity, but a cutaneous sign of mosaicism;Küster;Am J Med Genet,1999
5. Hypomelanosis of Ito: Diagnostic criteria and report of 41 cases;Ruiz-Maldonado;Pediatr Dermatol,1992
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1. Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism;Frontiers in Genetics;2024-04-16
2. Fundus Pigmentary Whorls in a Patient With Mosaicism for Tetrasomy 3q;JAMA Ophthalmology;2021-08-01
3. Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes;Frontiers in Neurology;2020-12-08
4. Hypomelanosis of Ito;Journal of Pediatric Neurology;2018-08-20
5. Possible Correlation between Hypomelanosis of Ito and Wilms’ Tumor;Case Reports in Pediatrics;2018-07-16
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