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

Osteogenesis imperfecta

Osteogenesis imperfecta (OI) comprises a heterogeneous group of genetic disorders characterized by increased bone fragility, low bone mass, and susceptibility to bone fractures with variable severity.

Median cleft lip

A type of cleft lip presenting as a midline (median) gap in the upper lip.

Total: 1

(per page)

PMID (PMCID)
3078619	FEMALE	Child
	A rare patient with a false median cleft lip associated with multiple congenital anomalies.
	Ohtsuka H. Ann Plast Surg. 1986;17(2):155-60.
	A girl manifesting a false median cleft lip associated with hypertelorism, anophthalmos, hydranencephaly with holoprosencephaly, and osteogenesis imperfecta, among other disorders, survived and was fed mainly milk products up to the age of 11.