Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines.
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| Title: | Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines. |
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| Authors: | Feng YQ; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China., Li WT; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China.; Department of Clinical Laboratory, Jiangxi Provincial Children's Hospital, Nanchang, China., Zou HY; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China., Xu QB; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China., Yang L; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China. |
| Source: | Translational pediatrics [Transl Pediatr] 2026 Jun 30; Vol. 15 (6), pp. 222. Date of Electronic Publication: 2026 May 20. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: AME Publishing Company Country of Publication: China NLM ID: 101649179 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2224-4344 (Print) Linking ISSN: 22244336 NLM ISO Abbreviation: Transl Pediatr Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42433928 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Feng+YQ%22">Feng YQ</searchLink>; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China.<br /><searchLink fieldCode="AU" term="%22Li+WT%22">Li WT</searchLink>; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China.; Department of Clinical Laboratory, Jiangxi Provincial Children's Hospital, Nanchang, China.<br /><searchLink fieldCode="AU" term="%22Zou+HY%22">Zou HY</searchLink>; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China.<br /><searchLink fieldCode="AU" term="%22Xu+QB%22">Xu QB</searchLink>; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China.<br /><searchLink fieldCode="AU" term="%22Yang+L%22">Yang L</searchLink>; Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital, Nanchang, China.; Department of Endocrinology, Metabolism and Genetics, The Affiliated Children's Hospital of Nanchang Medical College, Nanchang, China. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101649179%22">Translational pediatrics</searchLink> [Transl Pediatr] 2026 Jun 30; Vol. 15 (6), pp. 222. <i>Date of Electronic Publication: </i>2026 May 20. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22AME+Publishing+Company%22">AME Publishing Company </searchLink><i>Country of Publication: </i>China <i>NLM ID: </i>101649179 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>2224-4344 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222244336%22">22244336 </searchLink><i>NLM ISO Abbreviation: </i>Transl Pediatr <i>Subsets: </i>PubMed not MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42433928 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.21037/tp-2026-0264 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 222 Titles: – TitleFull: Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Feng YQ – PersonEntity: Name: NameFull: Li WT – PersonEntity: Name: NameFull: Zou HY – PersonEntity: Name: NameFull: Xu QB – PersonEntity: Name: NameFull: Yang L IsPartOfRelationships: – BibEntity: Dates: – D: 30 M: 06 Text: 2026 Jun 30 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 2224-4344 Numbering: – Type: volume Value: 15 – Type: issue Value: 6 Titles: – TitleFull: Translational pediatrics Type: main |
| ResultId | 1 |
