Autor(en)
Linhares, Natália D; Valadares, Eugênia R; da Costa, Silvia S; Arantes, Rodrigo R; de Oliveira, Luiz Roberto; Rosenberg, Carla; Vianna-Morgante, Angela M; Svartman, Marta
Titel
Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization
Teil von
  • Meta Gene, 2016-09, Vol.9, p.185-190
Ort / Verlag
Netherlands: Elsevier B.V
Links zum Volltext
Quelle
Free Medical Journals
Beschreibungen
We report on a 16-year-old boy with a maternally inherited ~18.3 Mb Xq13.2-q21.31 duplication delimited by aCGH. As previously described in patients with similar duplications, his clinical features included intellectual disability, developmental delay, speech delay, generalized hypotonia, infantile feeding difficulties, self-injurious behavior, short stature and endocrine problems. As additional findings, he presented recurrent seizures and pubertal gynecomastia. His mother was phenotypically normal and had completely skewed inactivation of the duplicated X chromosome, as most female carriers of such duplications. Five previously reported patients with partial Xq duplications presented duplication breakpoints similar to those of our patient. One of them, a fetus with multiple congenital abnormalities, had the same cytogenetic duplication breakpoint. Three of the reported patients shared many features with our proband but the other had some clinical features of the Prader-Willi syndrome. It was suggested that ATRX overexpression could be involved in the major clinical features of patients with partial Xq duplications. We propose that this gene could also be involved with the obesity of the patient with the Prader-Willi-like phenotype. Additionally, we suggest that the PCDH11X gene could be a candidate for our patient's recurrent seizures. In males, the Xq13-q21 duplication should be considered in the differential diagnosis of Prader-Willi syndrome, as previously suggested, and neuromuscular diseases, particularly mitochondriopathies. •We report a boy with inherited Xq13.2-q21.31 duplication.•As additional findings, the patient presented seizures and pubertal gynecomastia.•We compared our patient phenotype with five similar previously reported patients.•We propose novel roles for ATRX gene related to Prader-Willi-like phenotype.•The PCDH11X gene may be associated with recurrent seizures in dup(X) patients.
Format
Sprache(n)
Englisch
Identifikator(en)
ISSN: 2214-5400
ISSN: 2214-5400
DOI: 10.1016/j.mgene.2016.07.004
Links zum Inhalt
Schlagwörter
ATRX protein, Mitochondrial disease, PCDH11X protein, Prader-Willi syndrome, Xq13-q21 duplication
Systemstelle
Signatur

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