Partial Epilepsy and 47,XXX Karyotype: Report of Four Cases
Overview
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Epilepsy is a common finding in chromosomal imbalances, but only a few chromosome abnormalities have a characteristic electro-clinical pattern. Trisomy X is one of the most common sex chromosome abnormalities in females, and is associated with considerable phenotypic variability. This report describes four 47,XXX females with mental deficiency and epilepsy. Although a specific electro-clinical pattern could not be defined, the epileptic phenotypes of these patients share many features; we suggest that the association 47,XXX/epilepsy/mental retardation may not be coincidental. This report also enlarges the clinical spectrum of the 47,XXX phenotype. Moreover, these observations highlight the critical role of chromosome X in epilepsy and mental retardation.
Gschwind M, Zima B, Nedeltchev K, van Mierlo P, Ruegg S J Clin Neurol. 2022; 18(1):96-98.
PMID: 35021284 PMC: 8762506. DOI: 10.3988/jcn.2022.18.1.96.
Adaptive functioning in children and adolescents with Trisomy X: An exploratory analysis.
Wigby K, Cordeiro L, Wilson R, Angkustsiri K, Simon T, Tartaglia N Am J Med Genet C Semin Med Genet. 2020; 184(2):456-468.
PMID: 32548885 PMC: 8363475. DOI: 10.1002/ajmg.c.31803.
Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.
Wigby K, DEpagnier C, Howell S, Reicks A, Wilson R, Cordeiro L Am J Med Genet A. 2016; 170(11):2870-2881.
PMID: 27644018 PMC: 6501572. DOI: 10.1002/ajmg.a.37688.
Generalized epilepsy in a patient with mosaic Turner syndrome: a case report.
Jhang K, Chang T, Chen M, Liu C J Med Case Rep. 2014; 8:109.
PMID: 24694237 PMC: 4008388. DOI: 10.1186/1752-1947-8-109.
A review of trisomy X (47,XXX).
Tartaglia N, Howell S, Sutherland A, Wilson R, Wilson L Orphanet J Rare Dis. 2010; 5:8.
PMID: 20459843 PMC: 2883963. DOI: 10.1186/1750-1172-5-8.