Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Duodenal atresia

Duodenal atresia is an embryopathy of the cranial intestine that leads to a complete absence of the duodenal lumen.

Micrognathia

Developmental hypoplasia of the mandible.

Total: 1

(per page)

PMID (PMCID)
30351808	FEMALE	Infant
	[Difficult Airway Management in a Low Birth Weight Infant Using an Upper Gastrointestinal Endoscope].
	Sada Y, Taniguchi A, Miyamoto Y, Kitagawa H, Kinoucmi K. Masui. 2016;65(11):1173-1175.
	A 1-day-old female weighing 1.8 kg having micrognathia, lateral facial cleft, and bilateral microtia suggestive of Goldenhar syn- drome complicated with total anomalous pulmonary venous connection was scheduled for surgical repair of duodenal atresia.