Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia
ABSTRACT Saul Wilson syndrome is an extremely rare genetic disorder caused by heterozygous de novo mutations in the COG4 gene. We report the first case from Saudi Arabia with previously unreported facial dysmorphic features, expanding the known phenotypic spectrum and emphasizing the importance of recognizing phenotypic variability in rare disorders.
Saad A. Bin Owaimer +4 more
wiley +1 more source
Examining Transcriptomic Markers Associated With Neutrophil Extracellular Traps to Predict Mortality Risk in Neonatal Sepsis. [PDF]
Shaw D +4 more
europepmc +1 more source
Primary Repair of a Jejunal Atresia With Christmas Tree Deformity in a Preterm Infant
ABSTRACT Although uncommon in the general population, jejunoileal atresia (JIA) is a common cause of intestinal obstruction in infants. This congenital anomaly may cause a substantial reduction in intestinal length, enhancing the likelihood of short bowel syndrome and intestinal failure.
Dennis Machaku +5 more
wiley +1 more source
Transcriptomic mortality signature defines high-risk neonatal sepsis endotype. [PDF]
Al Gharaibeh FN +4 more
europepmc +1 more source
C-reactive Protein Versus Procalcitonin in the Early Diagnosis of Neonatal Sepsis: A Systematic Review. [PDF]
Sundara SV +6 more
europepmc +1 more source
Neonatal Sepsis: A Comprehensive Review. [PDF]
Kariniotaki C +5 more
europepmc +1 more source
Clinical and Microbiological Profile of Culture-Positive Neonatal Sepsis in a Tertiary Care Center in North India. [PDF]
Kartik K +5 more
europepmc +1 more source
Correction: <i>'</i>Epidemiology of early-onset neonatal sepsis in Qatar, 2015-2022: a multicentre retrospective cohort study'. [PDF]
europepmc +1 more source

