Omphalocele

Omphalocele is an embryopathy classified in the group of abdominal celosomias and is characterized by a large hernia of the abdominal wall, centered on the umbilical cord, in which the protruding viscera are protected by a sac.

Hepatomegaly

Abnormally increased size of the liver.


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PMID (PMCID)
29557630
 OTHER
[Surgical treatment of macroglossia in Beckwith-Wiedemann syndrome: case report].
Roa Rojas P, Arango Fernandez H, Rebolledo Cobos M, Harris Ricardo J.
Arch Argent Pediatr. 2018;116(2):e341-e345.
Beckwith-Wiedemann syndrome is a rare congenital condition, characterized by presenting macroglossia, defects of the abdominal wall, hemihypertrophy, omphalocele, neonatal hypoglycemia, umbilical hernia, hepatomegaly, cardiac abnormalities, among others.
11840663
 FEMALE Infant, Newborn
[A neonate with Beckwith-Wiedemann syndrome who developed upper airway obstruction after glossopexy].
Kotoku R, Kinouchi K, Fukumitsu K, Taniguchi A.
Masui. 2002;51(1):46-8.
She was delivered at 31 weeks of gestation with 2480 g and was diagnosed as Beckwith-Wiedeman syndrome, manifesting macroglossia, hepatomegaly, nephromegaly and omphalocele.