دورية أكاديمية
A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia.
| العنوان: | A novel GRK2 variant in a patient with Jeune asphyxiating thoracic dysplasia accompanied by Morgagni hernia. |
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| المؤلفون: | Şimşek-Kiper PÖ; Department of Pediatrics, Division of Pediatric Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey., Karaosmanoğlu B; Department of Medical Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey., Taşkıran EZ; Department of Medical Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey., Türer ÖB; Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey., Utine GE; Department of Pediatrics, Division of Pediatric Genetics, Hacettepe University Faculty of Medicine, Ankara, Turkey., Soyer T; Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey. |
| المصدر: | American journal of medical genetics. Part A [Am J Med Genet A] 2024 Sep; Vol. 194 (9), pp. e63629. Date of Electronic Publication: 2024 Apr 22. |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: Hoboken, N.J. : Wiley-Blackwell Original Publication: Hoboken, N.J. : Wiley-Liss, c2003- |
| مواضيع طبية MeSH: | Ellis-Van Creveld Syndrome*/genetics , Ellis-Van Creveld Syndrome*/pathology , G-Protein-Coupled Receptor Kinase 2*/genetics , Hernias, Diaphragmatic, Congenital*/genetics , Hernias, Diaphragmatic, Congenital*/diagnostic imaging , Hernias, Diaphragmatic, Congenital*/pathology, Female ; Humans ; Exome Sequencing ; Mutation ; Phenotype ; Infant |
| مستخلص: | Skeletal ciliopathies constitute a subgroup of ciliopathies characterized by various skeletal anomalies arising from mutations in genes impacting cilia, ciliogenesis, intraflagellar transport process, or various signaling pathways. Short-rib thoracic dysplasias, previously known as Jeune asphyxiating thoracic dysplasia (ATD), stand out as the most prevalent and prototypical form of skeletal ciliopathies, often associated with semilethality. Recently, pathogenic variants in GRK2, a subfamily of mammalian G protein-coupled receptor kinases, have been identified as one of the underlying causes of Jeune ATD. In this study, we report a new patient with Jeune ATD, in whom exome sequencing revealed a novel homozygous GRK2 variant, and we review the clinical features and radiographic findings. In addition, our findings introduce Morgagni hernia and an organoaxial-type rotation anomaly of the stomach and midgut malrotation for the first time in the context of this recently characterized GRK2-related skeletal ciliopathy. (© 2024 Wiley Periodicals LLC.) |
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| فهرسة مساهمة: | Keywords: GRK2; Morgagni hernia; exome sequencing; gastrointestinal malrotation; skeletal ciliopathy |
| المشرفين على المادة: | EC 2.7.11.16 (G-Protein-Coupled Receptor Kinase 2) EC 2.7.11.15 (GRK2 protein, human) |
| SCR Disease Name: | Jeune syndrome |
| تواريخ الأحداث: | Date Created: 20240422 Date Completed: 20240809 Latest Revision: 20240814 |
| رمز التحديث: | 20240815 |
| DOI: | 10.1002/ajmg.a.63629 |
| PMID: | 38647386 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.63629 |