epidermal-growth-factor and Neural-Tube-Defects

Holoprosencephaly is addressed under the following headings: alobar, semilobar, and lobar holoprosencephaly; arrhinencephaly; agenesis of the corpus callosum; pituitary abnormalities; hindbrain abnormalities; syntelencephaly; aprosencephaly/atelencephaly; neural tube defects; facial anomalies; median cleft lip; minor facial anomalies; single maxillary central incisor; holoprosencephaly-like phenotype; epidemiology; genetic causes of holoprosencephaly; teratogenic causes of holoprosencephaly; SHH mutations; ZIC2 mutations; SIX3 mutations; TGIF mutations; PTCH mutations; GLI2 mutations; FAST1 mutations; TDGF1 mutations; and DHCR7 mutations.

Topics: Epidermal Growth Factor; Eye Proteins; Face; Forkhead Transcription Factors; GPI-Linked Proteins; Hedgehog Proteins; Holoprosencephaly; Homeobox Protein SIX3; Homeodomain Proteins; Humans; Intercellular Signaling Peptides and Proteins; Kruppel-Like Transcription Factors; Membrane Glycoproteins; Mutation; Neoplasm Proteins; Nerve Tissue Proteins; Neural Tube Defects; Nuclear Proteins; Oxidoreductases Acting on CH-CH Group Donors; Patched Receptors; Patched-1 Receptor; Receptors, Cell Surface; Repressor Proteins; Transcription Factors; Zinc Finger Protein Gli2