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Lysosomal storage disorders (LSD) are a group of inherited metabolic diseases that contribute to nonimmune hydrops fetalis (NIHF). Our objective was to review the pooled exome sequencing (ES) diagnostic yield of LSD in NIHF cases. We expanded our previous meta-analysis and updated our search strategy of prenatal ES studies from 1/1/2000 to 8/1/2024. Cases with LSD gene variants were reviewed. Variants were curated based on the current American College of Medical Genetics and Genomics and ClinGen guidelines. Forty-one ES studies met our inclusion criteria. A total of 207/558 NIHF cases yielded a positive diagnosis by ES. LSD cases represented 27/558 (5%) of all clinically diagnosed NIHF cases that had ES. Rate of LSD among NIHF cases with positive genetic diagnosis by ES was 27/207 (13%). The 27 diagnostic variants and 4 additional variants of uncertain significance (VUS) were identified in 9 different LSD genes. All variants were inherited with a recurrence risk of 25%. Mucopolysaccharidosis type VII (MPS VII) was most prevalent (14/27, 52%). Also, the 4 cases with VUS were identified in the GUSB gene. Most cases (21/31, 68%) were isolated NIHF. Hydrops recurrence when reported was present in 75% (15/20) of cases. Consanguinity was reported in 57% (12/21) of cases. In conclusion, 5% of all NIHF cases received a genetic diagnosis of LSD by ES. Thirteen percent of NIHF cases that received a genetic diagnosis by ES were attributable to LSD, with MPS VII being the most prevalent condition. Pairing ES results with enzymatic studies can aid variant interpretation and could have potentially upgraded some of the 4 VUS cases, leading to a higher LSD diagnostic yield. Most cases of LSD presenting as NIHF manifest prenatally as isolated NIHF. High rate of NIHF recurrence and consanguinity highlight importance of genetic counseling and testing for LSD.
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http://dx.doi.org/10.1186/s13023-025-03851-9 | DOI Listing |
Genes (Basel)
August 2025
Department of Obstetrics and Gynaecology, Podobnik Special Hospital, Ul. Sveti Duh 112, 10000 Zagreb, Croatia.
Background/objectives: Cystic hygroma is a congenital lymphatic malformation often identified during early pregnancy and frequently associated with chromosomal abnormalities and adverse outcomes. We aimed to appraise the genetic and clinical characteristics of fetuses diagnosed with cystic hygroma in the first/early second trimester, assess the resolution patterns in chromosomally normal cases, and provide insights into prognosis-based on data collected over a 30-year period.
Methods: A retrospective cohort study was conducted on 405 consecutive fetuses diagnosed with nuchal cystic hygroma between 8.
Fetal Diagn Ther
August 2025
Hereditary pyropoikilocytosis (HPP) is a rare genetic disorder causing severe fetal anemia, often leading to hydrops fetalis. This study evaluates intrauterine blood transfusion (IUT) efficacy and associated genetic mutations in Northeastern Thai patients. Eight fetuses with hydrops fetalis were identified between 17 and 30+6 weeks' gestation, with initial hematocrit levels of 8.
View Article and Find Full Text PDFEur J Pediatr Surg
September 2025
Department of Pediatric Surgery, University Medical Centre Mannheim, Mannheim, BW, Germany.
Congenital pulmonary airway malformation (CPAM) is a rare fetal lung anomaly characterized by cystic lesions that can impede lung development. While smaller lesions may remain asymptomatic and are managed postnatally, larger lesions can cause severe complications such as mediastinal shift and hydrops fetalis. Fetal surgery may be indicated in these cases.
View Article and Find Full Text PDFJ Pers Med
August 2025
1st Department of Cardiology, AHEPA Hospital, School of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Fetal tachyarrhythmias, particularly supraventricular tachycardia (SVT) and atrial flutter (AFL), pose significant clinical challenges, especially when complicated by hydrops fetalis. This article provides a comprehensive review of the tachyarrhythmia types, the diagnostic modalities applied, and the therapeutic strategies followed in fetal tachyarrhythmias. Diagnostic techniques such as M-mode echocardiography and fetal magnetocardiography (fMCG) are highlighted for their capacity to provide real-time, high-quality assessments of fetal cardiac rhythms.
View Article and Find Full Text PDFEur J Pediatr
August 2025
Department of Neonatology, Amalia Children's Hospital, Radboud University Medical Center, Nijmegen, the Netherlands.
Unlabelled: Central conducting lymphatic anomaly (CCLA) is a rare and potentially life-threatening vascular malformation characterized by impaired central lymphatic flow. Hydrops fetalis and congenital hydro-/chylothorax are common neonatal presentations; however, diagnosing CCLA poses challenges and requires advanced imaging. Management typically includes supportive therapies with limited effect, such as medium-chain triglyceride (MCT) diet, octreotide or propranolol, and thoracic drainage.
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