To analyze the ocular and systemic clinical features of children with CHARGE syndrome, which is a congenital autosomal dominant developmental disorder mainly characterized by coloboma (C), heart disease (H), atresia choanae (A), retarded growth and central nervous system anomalies (R), genital hypoplasia (G), and ear anomalies and deafness (E). This was a retrospective caseseries study. Eight children (16 eyes) with CHARGE syndrome who visited the Department of Ophthalmology, Xijing Hospital, Air Force Medical University from January 2018 to December 2022 were included in this study. All 8 children underwent ocular and systemic examinations; 4 children underwent genetic testing. The basic birth conditions, medical history, and family history of the children were recorded in detail. The ocular and systemic clinical manifestations of the children were summarized, and the results of gene sequencing were analyzed. Among the 8 children, 5 were male and 3 were female. The age at the first ophthalmological visit ranged from 2 months to 15 years. Five children were first diagnosed in the ophthalmology department, and 3 were referred from the otolaryngology department. All 8 children had ocular abnormalities such as characteristic, asymmetric, and congenital choroidal coloboma. Among them, the proportion of children with hearing impairment was 7/8, ear malformation was 8/8, developmental delay was 7/8, heart malformation was 5/8, intellectual disability was 3/8, choanal stenosis was 1/8, renal malformation was 1/8, and skeletal malformation was 1/8. All 4 children who underwent genetic testing were found to have mutations in the chromodomain helicase DNA-binding protein 7 (CHD7) gene, and all were pathogenic de novo mutations. The clinical manifestations of children with CHARGE syndrome are diverse and highly associated with CHD7 gene mutations. The main ocular manifestation is tissue coloboma, and it is often accompanied by severe malformations in multiple organ systems such as the ears, heart, nervous system, and endocrine system.
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http://dx.doi.org/10.3760/cma.j.cn112142-20241130-00548 | DOI Listing |
Nat Commun
March 2025
School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel.
Allele-specific DNA methylation reflects genetic variation and parentally-inherited changes, and is involved in gene regulation and pathologies. Yet, our knowledge of this phenomenon is largely limited to blood. Here we present a comprehensive atlas of allele-specific DNA methylation using deep whole-genome sequencing across 39 normal human cell types.
View Article and Find Full Text PDFGlycobiology
March 2025
Department of Biochemistry, Case Western Reserve University, Cleveland, OH 44106, United States.
Mucin type O-glycan core elongation is typically performed by the C1GALT1, B3GNT6, and ST6GalNAc-I/-II O-glycosyltransferases. These enzymes target the Tn antigen (GalNAc-O-Thr/Ser) dictating the fate of O-glycan elongation, playing important roles in health and disease. Changes in transferase expression and glycan structure are commonly associated with diseases such as cancer, Tn-syndrome, and ulcerative colitis.
View Article and Find Full Text PDFBr J Nurs
March 2025
Senior Charge Nurse, Adult Critical Care Unit, St Bartholomew's Hospital, Barts Health NHS Trust, London.
The approval, introduction, and provision of chimeric antigen receptor (CAR) T-cell therapy in the UK NHS presents a innovative and revolutionary approach in cancer treatment and management. CAR T-cell therapy is a highly specialised and personalised type of immunotherapy that involves reprogramming a patient's immune system by synthetically modifying their T-cells to specifically target and eliminate cancer cells. This therapy offers the potential to cure malignancies that were previously deemed incurable or refractory to conventional chemotherapy.
View Article and Find Full Text PDFZhonghua Yan Ke Za Zhi
March 2025
Department of Ophthalmology, Xijing Hospital, Air Force Military Medical University, Eye Institute of Chinese PLA, Xi'an 710032, China.
To analyze the ocular and systemic clinical features of children with CHARGE syndrome, which is a congenital autosomal dominant developmental disorder mainly characterized by coloboma (C), heart disease (H), atresia choanae (A), retarded growth and central nervous system anomalies (R), genital hypoplasia (G), and ear anomalies and deafness (E). This was a retrospective caseseries study. Eight children (16 eyes) with CHARGE syndrome who visited the Department of Ophthalmology, Xijing Hospital, Air Force Medical University from January 2018 to December 2022 were included in this study.
View Article and Find Full Text PDFItal J Pediatr
March 2025
Operative Unit of Neonatology, IRCCS Ospedale Policlinico San Martino, Genoa, 16132, Italy.
Congenital ocular anomalies significantly contribute to global disability, with 15-20% of infant blindness attributed to these anomalies. This study examined anophthalmia, microphthalmia, and coloboma (AMC) through collaborative neonatology and ophthalmology care.The global prevalence of AMC varies: anophthalmia at 0.
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