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PedAM

Pediatric Disease Annotations & Medicines




Disease cleft lip
Phenotype |cleft palate
Sentences 332
PubMedID- 25808365 Rs1801133c>t polymorphism in mthfr is a risk factor for nonsyndromic cleft lip with or without cleft palate in the brazilian population.
PubMedID- 26402724 Participants: the study sample consisted of 189 case-parent trios of nonsyndromic cleft lip with or without cleft palate (nscl+/-p), 107 case-parent trios of nonsyndromic cleft palate (nscp), 318 isolated samples of nscl+/-p, 189 isolated samples of nscp, and 599 healthy controls.
PubMedID- 21132229 Results: high frequencies regional analysis showed the following significant results: pam: severe hypospadias; cen: spina bifida, microtia, cleft lip with cleft palate, polycystic kidney, postaxial polydactyly and down syndrome; cuy: postaxial polydactyly; noa: omphalocele, gastroschisis, cleft lip without cleft palate, cleft lip with cleft palate, anorectal atresia/stenosis, indeterminate sex, preaxial polydactyly and pectoral agenesis; pat: cleft lip without cleft palate.
PubMedID- 26507587 Interactions between rad51 rs1801321 and maternal cigarette smoking as risk factor for nonsyndromic cleft lip with or without cleft palate.
PubMedID- 20878909 Stratification by type of surveillance system showed that active programs had a higher prevalence of anencephaly, anophthalmia/microphthalmia, cleft lip with or without cleft palate, reduction defect of upper limbs, and trisomy 18.
PubMedID- 25704602 Identification of functional variants for cleft lip with or without cleft palate in or near pax7, fgfr2, and nog by targeted sequencing of gwas loci.
PubMedID- 26110153 Background: non-syndromic cleft lip with or without cleft palate (nscl/p) is one of the most common congenital abnormalities of the orofacial region with a multifactorial etiology.
PubMedID- 22549767 To demonstrate the application, we apply our method to candidate gene sequencing data from a german case-control study on nonsyndromic cleft lip with or without cleft palate.
PubMedID- 22363504 Clptm1 is a candidate gene for cleft lip with or without cleft palate malformation [19], [20].
PubMedID- 22471252 The aim of this study was to assess the accuracy of prenatal diagnosis of cleft lip with or without cleft palate, and isolated cleft palate (icp), in our catchment area.
PubMedID- 22723972 For haplotype analysis, we used a sliding-window approach and assessed isolated cleft lip with or without cleft palate (icl/p) separately from isolated cleft palate only (icpo).
PubMedID- 22345991 Background: cleft lip with or without cleft palate (cl/p) is the most frequent craniofacial malformation seen in man.
PubMedID- 21381882 Cchd, anencephaly, spina bifida, congenial diaphragmatic hernia (cdh), omphalocele, gastroschisis, limb defects, cleft lip with or without cleft palate (cl/p) and isolated cleft palate were evaluated.
PubMedID- 23028347 In a recent candidate gene study carried out in two independent european population samples, we investigated a potential association between risk alleles for non-syndromic cleft lip with or without cleft palate (nscl/p) and nose width and facial width in the normal population [20].
PubMedID- 21113916 The distribution of clefts was as follows: 18 (29%) cleft lip, 25 (40%) cleft lip with cleft palate, 17 (27%) cleft palate only, one median cleft and one atypical cleft.
PubMedID- 23776525 Non-syndromic cleft lip with or without cleft palate (nscl/p [omim %119530]) is one of the most common congenital defects.
PubMedID- 21760670 Compared cleft palate patients with cleft lip, alveolus and palate patients, but there was no cleft lip group included.
PubMedID- 22090755 Stevenson and johnson[16] stated that cleft lip with or without cleft palate is more common in males with the ratio of approximately 2:1 over females; our study correlates the above study.
PubMedID- 20020508 Nonsyndromic cleft lip with or without cleft palate (clp) is a frequent craniofacial malformation caused by both genetic and environmental factors.
PubMedID- 23903689 Forms of nsoc include cleft lip with or without cleft palate (cl/p)and cleft palate only (cpo) (2).
PubMedID- 21834038 Moreover, the apparent protection against cleft lip with or without cleft palate (cl/p), cleft lip with cleft palate (clp), and cleft lip only (clo) was also identified in stratified analysis.
PubMedID- 26540672 The aim of the investigation was to replicate previous studies reporting evidence of association between polymorphisms of folate related genes and the occurrence of non-syndromic cleft lip with or without cleft palate (nscl/p), using three independent samples of different ancestry: from tibet, bangladesh and iran, respectively.
PubMedID- 21781437 Maternal c677t mthfr genotype has been identified as important factor in cleft lip with or without cleft palate (cl/p) etiology.
PubMedID- 21254359 Background: nonsyndromic cleft lip with or without cleft palate (nsclp) is a common complex birth defect.
PubMedID- 26336015 The prevalence of cleft lip with or without cleft palate was 0.9 per 10000 children, achondroplasia was 0.7 per 10000, and dandy-walker syndrome was 0.4 per 10000.
PubMedID- 24375841 Objective: to investigate trends in prenatal diagnosis and termination of pregnancy rates in cases of fetal cleft lip with or without cleft palate (cl +/- p), before and after the introduction in the netherlands of the 20-week anomaly scan in 2007, and to assess the accuracy of this scan for the diagnosis of facial clefts.
PubMedID- 22415108 Methods: in a prospective cohort of 240,244 women enrolled between 1993 and 1995 in 1 northern and 2 southern provinces in china, we examined the risk of nonsyndromic cleft lip with or without cleft palate (cl/p) and cleft palate alone (cp) in relation to maternal use of 400 mug of folic acid without other vitamins.
PubMedID- 20681225 There was bilateral cleft lip with cleft palate.
PubMedID- 26140186 cleft lip with or without cleft palate (cl/p) is among the most common orofacial congenital anomalies in the world 1. several epidemiological studies have reported the prevalence of cleft lip and/or palate in iran and worldwide 2–8.
PubMedID- 24304547 Analyses evaluating cleft lip (with or without cleft palate) and cleft palate separately were similar to analyses evaluating both oral cleft defects combined, except the or for cleft palate and average 1st trimester tce exposure > mcl was elevated (cleft palate or = 1.4, 95% ci: 0.3-7.0 versus the combined oral clefts or = 0.8, 95% ci: 0.2-3.0), but this was based on two exposed cases.
PubMedID- 22565872 Although muenke syndrome is the most common syndromic form of craniosynostosis, the frequency of oral and palatal anomalies including high-arched palate, cleft lip with or without cleft palate has not been documented in a patient series of muenke syndrome to date.
PubMedID- 25884320 For non-syndromic cl ± p (cleft lip with or without cleft palate), the recurrence risk for a subsequent sibling is considered to be 3-5% [49,51].
PubMedID- 24454740 Because of suggested differences in genetic origin [1], [5], [22], we also analysed oral clefts subdivided into cleft lip with or without cleft palate (icd-10 codes q36 and q37) and isolated cleft palate (q35).
PubMedID- 22754157 cleft lip with or without cleft palate occurs in approximately 0.91–2.69 in 1000 white births.
PubMedID- 23008150 Expression and mutation analyses implicate arhgap29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
PubMedID- 21408183 However, the importance of cncs in disease has been documented in several disorders including preaxial polydactyly [15], [16], [17], human nscl/p (non syndromic cleft lip with or without cleft palate) [18] holoprosencephaly [19] and pierre robin sequences (a subgroup of cleft palate) [20].
PubMedID- 24531247 cleft lip with or without cleft palate (cl/p) is a relatively common craniofacial malformation involving bony and soft-tissue disruptions of the nasolabial and dentoalveolar regions.
PubMedID- 24706492 Nonsyndromic cleft lip with or without cleft palate: increased burden of rare variants within gremlin-1, a component of the bone morphogenetic protein 4 pathway.
PubMedID- 21612398 On the contrary, mthfr 1298 ac and 1298 ac/cc appeared to be protective against cleft lip with cleft palate.
PubMedID- 20023658 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.
PubMedID- 22759670 cleft lip with or without cleft palate (clp) and cleft palate only (cp) are severe disruptions affecting orofacial structures.
PubMedID- 26043427 Association between polymorphisms at the grem1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the polish population.
PubMedID- 22754168 cleft lip (with or without cleft palate) has been seen in nearly all cases of popliteal pterygium syndrome, whereas cleft palate is present in only 41% of multiple pterygium syndrome.
PubMedID- 20087401 Isolated cleft lip with or without cleft palate and cleft palate are among the most common human birth defects.
PubMedID- 23055981 cleft lip, with or without cleft palate, and isolated cleft palate occur with a frequency of 1–2 in thousand live births.
PubMedID- 25786657 Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in europeans.
PubMedID- 20526256 Background: the purpose of this study is to follow the familial incidence of non-syndromic or isolated cleft lip, with or without cleft palate (nscl/p), and to analyze the relationships between the type of nscl/p in the affected individual and his/her parent, looking at children in the first grade.
PubMedID- 22875508 Objective: to explore the association between parental genetic polymorphism of methylenetetrahydrofolate reductase (mthfr) 677c/t and occurrence of nonsyndromic cleft lip with or without cleft palate (nscl/p) in offspring in shandong province.
PubMedID- 25885235 The cleft lip (with or without cleft palate) is more common in males, whereas isolated cleft palate is more common in females.
PubMedID- 23395979 Our findings suggest that the duplicated segment predisposes for cleft lip with or without cleft palate (cl/p), or any of the other phenotypic features presented by the patient.

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