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HOLOPROSENCEPHALY 4 (disorder)

Known as: HPE4, Holoprosencephaly 4, Holoprosencephaly Type 4 
A rare disorder caused by mutations in the TGIF gene mapped to chromosome 18p11.3. It is characterized by semilobar holoprosencephaly, hypotelorism… 
National Institutes of Health

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Broader (1)

Holoprosencephaly
TGIF, PRO63ARGTGIF, TYR59TERTGIF1 geneTGIF1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Alobar Holoprosencephaly with Duodenal Atresia: A Case Report
Introduction: Holoprosencephaly (HPE) is the most frequent malformation of the prosencephalon. It represents the absence or… 
2013
2013
Diagnóstico prenatal de holoprosencefalia
305 Revista Medica MD Volumen 4, numero 3; febrero abril 2013 unico y fusion de talamos; en esta variante encontramos la mayoria… 
2011
2011
How Can We Prevent Birth of Fetus With Holoprosencephaly? Anatomical and Embryological Aspects of Holoprosencephaly.
Objectives: Holoprosencephaly is a rare condition characterized by different degrees of fused ventricles of the brain resulting… 
2005
2005
CNS malformations: gene locations of known human mutations.
1997
1997
The human gene ZFP161 on 18p11.21-pter encodes a putative c-myc repressor and is homologous to murine Zfp161 (Chr 17) and Zfp161-rs1 (X Chr)
A clone from a lambda gt11 cDNA expression library of HeLa cells was isolated, sequenced, and shown to encode a new human zinc… 
1992
1992
偽性正中唇裂を伴う holoprosencephaly の手術経験と本邦報告例の統計的観察
1992
1992
本態性高Na血症を伴った lobar type holoprosencephaly の1例にみられた口蓋裂閉鎖術後の急性低Na血症性脳症
1978
1978
5. Holoprosencephaly の 2 例(第 11 回日本小児外科学会中国四国地方会)
1966
1966
Holoprosencephaly/arbinencephaly: A case with no biochemical adnormalities
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