Guidelines and recommendations for performance of the fetal echocardiogram: an update from the American Society of Echocardiography

AJ Moon-Grady, MT Donofrio, S Gelehrter… - Journal of the American …, 2023 - Elsevier
In 2004 the American Society of Echocardiography (ASE) guidelines and standards for the
performance of fetal echocardiography were published. 1 The writing group, commissioned …

A system‐based approach to the genetic etiologies of non‐immune hydrops fetalis

AH Mardy, SP Chetty, ME Norton… - Prenatal …, 2019 - Wiley Online Library
A wide spectrum of genetic causes may lead to nonimmune hydrops fetalis (NIHF), and a
thorough phenotypic and genetic evaluation are essential to determine the underlying …

Nonimmune hydrops fetalis

C Swearingen, ZA Colvin… - Clinics in …, 2020 - perinatology.theclinics.com
The term hydrops fetalis describes excessive, pathologic fluid accumulation within the fetal
soft tissues and body cavities. 1, 2 It is defined by the presence of 2 or more abnormal fluid …

Outcomes and predictors of perinatal mortality in fetuses with Ebstein anomaly or tricuspid valve dysplasia in the current era: a multicenter study

LR Freud, MC Escobar-Diaz, BT Kalish, R Komarlu… - Circulation, 2015 - Am Heart Assoc
Background—Ebstein anomaly and tricuspid valve dysplasia are rare congenital tricuspid
valve malformations associated with high perinatal mortality. The literature consists of small …

[HTML][HTML] Nonimmune hydrops fetalis: identifying the underlying genetic etiology

TN Sparks, K Thao, BR Lianoglou, NM Boe… - Genetics in …, 2019 - Elsevier
Purpose Numerous etiologies may lead to nonimmune hydrops fetalis (NIHF), and the
underlying cause often remains unclear. We aimed to determine the proportion of NIHF …

Epidemiology of live born infants with nonimmune hydrops fetalis—insights from a population-based dataset

MA Steurer, S Peyvandi, RJ Baer, T MacKenzie… - The Journal of …, 2017 - Elsevier
Objective To evaluate the incidence, etiology, and 1-year mortality of nonimmune hydrops
fetalis (NIHF) and to identify risk factors for mortality in a contemporary population-based …

Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects

A Herzeg, B Borges, BR Lianoglou… - Prenatal …, 2023 - Wiley Online Library
Lysosomal storage disorders (LSDs) are a group of monogenic condition, with many
characterized by an enzyme deficiency leading to the accumulation of an undegraded …

Tolerance induction and microglial engraftment after fetal therapy without conditioning in mice with Mucopolysaccharidosis type VII

QH Nguyen, RG Witt, B Wang, C Eikani… - Science Translational …, 2020 - science.org
Mucopolysaccharidosis type VII (MPS7) is a lysosomal storage disorder (LSD) resulting from
mutations in the β-glucuronidase gene, leading to multiorgan dysfunction and fetal demise …

Favorable outcomes after in utero transfusion in fetuses with alpha thalassemia major: a case series and review of the literature

EM Kreger, ST Singer, RG Witt, N Sweeters… - Prenatal …, 2016 - Wiley Online Library
Objective Alpha thalassemia major (ATM) is often fatal in utero due to severe hydrops fetalis.
Although in utero transfusions (IUTs) are increasingly used to allow fetal survival in ATM …

A broader perspective on anti-Ro antibodies and their fetal consequences—a case report and literature review

MR Popescu, A Dudu, C Jurcut, AM Ciobanu… - Diagnostics, 2020 - mdpi.com
The presence of maternal Anti-Ro/Anti-La antibodies causes a passively acquired
autoimmunity that may be associated with serious fetal complications. The classic example …