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

Myelomeningocele

Micrognathia

Developmental hypoplasia of the mandible.

Total: 1

(per page)

PMID (PMCID)
27309155	FEMALE	Adult
	Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses.
	Inan C, Sayn NC, Atl E, Ulusal S, Erzincan S, Uzun I, Gurkan H, Varol FG. Fetal Pediatr Pathol. 2016;35(5):339-343.
	It is accompanied by various abnormalities including congenital heart defects, lower extremity abnormalities, micrognathia, high arched palate, kyphoscoliosis, microcephaly, myelomeningocele, hernia and renal anomalies.