holoprosencephaly

holoprosencephaly
A congenital disorder involving insufficient division of the lobes of the brain during fetal development, resulting in skull and facial deformities ranging from minor cleft lip problems to cyclopia, in which a single eye develops where the nose would normally be.
See Also: alobar, semilobar, lobar, premaxillary agenesis, cyclopia, ethmocephaly, cebocephaly

Wikipedia foundation.

Игры ⚽ Нужен реферат?

Look at other dictionaries:

  • Holoprosencephaly — Classification and external resources Diagram depicting the main subdivisions of the embryonic vertebrate brain. ICD 10 Q …   Wikipedia

  • Holoprosencephaly — A disorder characterized by the failure of the prosencephalon (the forebrain of the embryo) to develop. During normal development, the forebrain is formed and the face begins to develop in the fifth and sixth weeks of pregnancy. Holoprosencephaly …   Medical dictionary

  • holotelencephaly — Holoprosencephaly associated with arrhinencephaly. [holo + telencephalon] …   Medical dictionary

  • Ethmocephaly — is a type of cephalic disorder caused by holoprosencephaly. Ethmocephaly is the least common facial anomaly. It consists of a proboscis separating narrow set eyes with an absent nose and microphthalmia (abnormal smallness of one or both eyes).… …   Wikipedia

  • Homeobox protein TGIF1 — TGFB induced factor homeobox 1, also known as TGIF1, is a human gene.cite web | title = Entrez Gene: TGIF1 TGFB induced factor homeobox 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=7050| accessdate = ] …   Wikipedia

  • 18p- — Classification and external resources OMIM 146390 18p is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 40,000 births. Contents …   Wikipedia

  • ZIC2 — Zic family member 2 (odd paired homolog, Drosophila), also known as ZIC2, is a human gene.cite web | title = Entrez Gene: ZIC2 Zic family member 2 (odd paired homolog, Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

  • SIX3 — Sine oculis homeobox homolog 3 (Drosophila), also known as SIX3, is a human gene.cite web | title = Entrez Gene: SIX3 sine oculis homeobox homolog 3 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… …   Wikipedia

  • Cyclopia — This article is about the congenital disorder. For other uses, see Cyclopia (disambiguation). Cyclopia Classification and external resources ICD 10 Q …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”