Top 10 similar words or synonyms for cleft_lip_palate

ectodermal_dysplasia    0.873460

aplasia    0.853769

aniridia    0.850376

ectrodactyly    0.841792

arthrogryposis    0.841042

dysmorphism    0.839873

macrocephaly    0.831043

microphthalmia    0.829124

wagr_syndrome    0.826732

marfan_syndrome    0.824589

Top 30 analogous words or synonyms for cleft_lip_palate

Article Example
Craniofacial team Craniofacial anomalies or syndromes are defined as congenital conditions other than cleft lip/palate, unless cleft lip/palate is a feature of another condition, anomaly or syndrome.
Yim–Ebbin syndrome It is also known as "amelia cleft lip palate hydrocephalus iris coloboma".
ARHGAP29 The 1p22 locus containing ARHGAP29 was associated with nonsydromic cleft lip/palate by genome wide association and meta-analysis. A follow-up study identified rare coding variants including a nonsense and a frameshift variant in patients with nonsydromic cleft lip/palate. The finding of ARHGAP29's role in craniofacial development was discovered after the adjacent ABCA4 gene lacked functional or expression data to support it as the etiologic gene for nonsydromic cleft lip/palate even though SNPs in the ABCA4 gene were associated with cleft lip/palate.
S. M. Balaji He was the first Indian to be the President of the 7th World Cleft Lip & Palate Congress held at Republic of Seychelles.
Cleft lip and cleft palate Many genes associated with syndromic cases of cleft lip/palate (see above) have been identified to contribute to the incidence of isolated cases of cleft lip/palate. This includes in particular sequence variants in the genes "IRF6", "PVRL1" and "MSX1". The understanding of the genetic complexities involved in the morphogenesis of the midface, including molecular and cellular processes, has been greatly aided by research on animal models, including of the genes "BMP4", "SHH", "SHOX2", "FGF10" and "MSX1".
Acrofrontofacionasal dysostosis Acrofrontofacionasal dysostosis is an extremely rare disorder, characterized by intellectual disability, short stature, hypertelorism, broad notched nasal tip, cleft lip/palate, postaxial camptobrachypolysyndactyly, fibular hypoplasia, and anomalies of foot structure.
Polydactyly Other syndromes including polydactyly include acrocallosal syndrome, basal cell nevus syndrome, Biemond syndrome, ectrodactyly-ectodermal dysplasias-cleft lip/palate syndrome, mirror hand deformity, Mohr syndrome, oral-facial-digital syndrome, Rubinstein-Taybi syndrome, short rib polydactyly, and VATER association.
Cleft lip and cleft palate Genetic factors contributing to cleft lip and cleft palate formation have been identified for some syndromic cases, but knowledge about genetic factors that contribute to the more common isolated cases of cleft lip/palate is still patchy.
MMP3 On the other hand, the 6A allele has been found to be associated with diseases characterized by insufficient MMP-3 expression due to a lower promoter activity of the 6A allele, such as progressive coronary atherosclerosis. The -1171 5A/6A variant has also been associated with congenital anomalies such as cleft lip and palate, where individuals with cleft lip/palate presented significantly more 6A/6A genotypes than controls. Recently, the MMP3 gene was shown to be down-regulated in individuals with cleft lip and palate when compared to controls, reinforcing the nature of cleft lip/palate as a condition resulting from insufficient or defective embryonic tissue remodeling.
Charles Jeter Jeter was born in Columbia, SC on August 30, 1973. He was born with a cleft lip & palate which has led to 26 corrective surgeries in his life. The first was at six weeks old and the final corrective surgery was in 1996 at age 23.