Important nomenclature changes for steatohepatitis (SH) have recently arisen to
systematically identify patient populations within appropriate categories of disease etiology …

Pediatric genetic and metabolic liver diseases comprise a broad spectrum of conditions and
represent the second most common indication for liver transplantation following biliary …

Background Neonatal hemophagocytic lymphohistiocytosis (nHLH), defined as HLH that
presents in the first month of life, is clinically devastating. There have been few large …

Classic alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a
rare congenital lung disorder presenting in the early neonatal period with refractory …

Abstract Purpose of Review Acute liver failure in neonates and early infancy is an
uncommon condition with varied etiology and high mortality rates. We attempt to review the …

The neonatal period is a peak time for the presentation of genetic disorders that can be
diagnosed using whole genome sequencing (WGS). While any one genetic disorder is …

X-Linked Lymphoproliferative Disease Associated Hemophagocytic Lymphohistiocytosis
Diagnosed Expeditiously With Ultra-Rapid Whole-Genome Sequencing X-Linked …