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Holoprosencephaly

Holoprosencephaly (HPE) is a complex brain malformation resulting from incomplete cleavage of the prosencephalon, occurring between the 18th and 28th day of gestation, and affecting both the forebrain and face, which results in neurological manifestations and facial anomalies of variable severity.

Hypopituitarism

Total: 1

(per page)

PMID (PMCID)
2325094	FEMALE
	Microphthalmia with single central incisor and hypopituitarism.
	Artman HG, Boyden E. J Med Genet. 1990;27(3):192-3.
	A patient is described with a new association of microphthalmia, single central incisor, and hypopituitarism believed to represent a holoprosencephaly malformation.