Results 241 to 250 of about 141,336 (294)

Saul Wilson Syndrome: A Case Report With New Features in Saudi Arabia

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
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

Primary Repair of a Jejunal Atresia With Christmas Tree Deformity in a Preterm Infant

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
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]

open access: yesFront Immunol
Al Gharaibeh FN   +4 more
europepmc   +1 more source

Neonatal sepsis.

open access: yesNorth Carolina medical journal, 1967
D Y, Sanders, H G, Cramblett
openaire   +1 more source

Neonatal Sepsis: A Comprehensive Review. [PDF]

open access: yesAntibiotics (Basel)
Kariniotaki C   +5 more
europepmc   +1 more source

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