Newborn whit a derivative chromosome X and ambiguous genitalia

Simão, Laurentino; Serafim, Sílvia; Brito, Filomena; Alves, Cristina; Silva, Marisa; Peliano, Ricardo; Ferreira, Cristina; Marques, Bárbara; Pedro, Sónia; Oliveira, Juliana; Branco, Tiago; Correia, Hildeberto

Publication

Newborn whit a derivative chromosome X and ambiguous genitalia

2019-11-14Conference object

dc.contributor.author	Simão, Laurentino
dc.contributor.author	Serafim, Sílvia
dc.contributor.author	Brito, Filomena
dc.contributor.author	Alves, Cristina
dc.contributor.author	Silva, Marisa
dc.contributor.author	Peliano, Ricardo
dc.contributor.author	Ferreira, Cristina
dc.contributor.author	Marques, Bárbara
dc.contributor.author	Pedro, Sónia
dc.contributor.author	Oliveira, Juliana
dc.contributor.author	Branco, Tiago
dc.contributor.author	Correia, Hildeberto
dc.date.accessioned	2020-05-22T19:31:43Z
dc.date.available	2020-05-22T19:31:43Z
dc.date.issued	2019-11-14
dc.description.abstract	Translocations involving the short arms of the X and Y in human chromosomes are uncommon. One of the primary functions of the X and Y chromosomes is gender phenotype determination. Here we report a newborn female with ambiguous genitalia and abnormal X chromosome. Karyotype was performed using the standard methods and Fluorescence in situ hybridization (FISH) directed for the SRY gene was used for confirmation of the clinical and cytogenetic suspicion. Chromosomal microarray analysis (CMA) was performed using CytoScan HD (Affimetrix®) to identified gains/loses on the der(X) chromosome. The analyse revealed one abnormal X chromosome in a female karyotype. Considering the ambiguous genitalia clinical information the abnormal X was considered to be compatible with a translocation X/Y. This was confirmed by the presence of signal for the SRY using FISH. CMA allowed to clarify a loss of 12.34 Mb at Xp22.33p22.2 and a gain of 7.41 Mb at Yp11.31p11.2 (ISCN = arr[GRCh37] Xp22.33p22.2(2703632_15050955)x1,Yp11.31p11.2(2650140_10059230)x1). The X deleted region includes several OMIM morbid genes, including CLCN4. Mutations in CLCN4 are associated with intellectual disability and impaired language development, and heterozygous females can be as severely affected as male. The gain on the Y encompasses nine OMIM genes, including the SRY gene, involved in the sexual male development. This additional information can be of great value for the child development. Translocations of segments of Y chromosome containing SRY are described in sexual reversion and true hermafroditism cases, which could explain the reason for referral for the newborn. Nevertheless, translocations between the X/Y chromosomes in females are expected to have a skewed inativation pattern in favour of the abnormal X and X-inativation studies could prove this likelihood. If a normal developmental of the child is observed over time this will be likely due to the preferable inativation of the abnormal X. Presently the child is about 1-year-old and she presents normal uterus, ovarian, and external genitalia, with absence of male gonads. No other clinical features have been identified.	pt_PT
dc.description.version	N/A	pt_PT
dc.identifier.uri	http://hdl.handle.net/10400.18/6755
dc.language.iso	eng	pt_PT
dc.peerreviewed	yes	pt_PT
dc.rights.uri	http://creativecommons.org/licenses/by-nc/4.0/	pt_PT
dc.subject	Translocation X/Y	pt_PT
dc.subject	Derivative Chromosome	pt_PT
dc.subject	CMA	pt_PT
dc.subject	CLCN4	pt_PT
dc.subject	Doenças Genéticas	pt_PT
dc.title	Newborn whit a derivative chromosome X and ambiguous genitalia	pt_PT
dc.type	conference object
dspace.entity.type	Publication
oaire.citation.conferencePlace	Coimbra, Potugal	pt_PT
oaire.citation.title	23nd Annual Meeting of the Portuguese Society of Human Genetics, 14-16 Novembro 2019	pt_PT
rcaap.rights	embargoedAccess	pt_PT
rcaap.type	conferenceObject	pt_PT