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1,757 Possible Causes for Cleft Palate, Congenital Heart Disease

  • Patau Syndrome

    […] lip, and cleft palate.[learningaboutelectronics.com] Most infants with trisomy 13 have congenital heart disease.[nlm.nih.gov] heart disease, blindness, severe mental retardation may complicate survival Please rate topic.[medbullets.com]

  • Velocardiofacial Syndrome

    PARTICIPANTS: Eight children with VCFS and five children with nonsyndromic cleft palate or VPD.[ncbi.nlm.nih.gov] Abstract We report on a child with congenital heart disease (atrial septal defect, ventricular septal defect, pulmonic stenosis), submucosal cleft palate, hypernasal speech[ncbi.nlm.nih.gov] BACKGROUND: Velocardiofacial syndrome (VCFS) is a disorder commonly associated with a characteristic facial appearance, congenital heart disease, and velopharyngeal insufficiency[ncbi.nlm.nih.gov]

  • Pierre Robin Syndrome

    Skeletal II jaw relation was observed in 32% of the children with isolated cleft palate.[ncbi.nlm.nih.gov] Abstract Congenital heart disease occurs in about 20 percent of patients with Pierre Robin syndrome.[ncbi.nlm.nih.gov] There are often signs of congenital heart disease, such as atrial septal defect (ASD), patent ductus arteriosus, ventricular septal defect (VSD).[doi.org]

  • CHARGE Syndrome

    Abstract Previously, we reported on a family with a new syndrome of cleft palate, coloboma, hypospadias, deafness, short stature, and radial synostosis.[ncbi.nlm.nih.gov] heart disease ) A : atresia (choanal) R : retardation (mental) G : genital hypoplasia E : ear abnormalities /deafness CHARGE syndrome is usually suspected at birth once multiple[radiopaedia.org] Lip /- Cleft Palate Cleft lip with or without cleft palate, cleft palate, submucous cleft palate Image of Repaired Cleft Lip 20% TE Fistula Esophageal atresia, Trancheo-esophageal[chargesyndrome.org]

  • Mandibulofacial Dysostosis

    palate.[ncbi.nlm.nih.gov] Extracraniofacial malformations include esophageal atresia, congenital heart disease, and radial ray abnormalities.[ncbi.nlm.nih.gov] Some association with congenital heart disease, TEF, and anal atresia. Radiologic manifestations Hypoplasia of the malar bones.[neuroradiologyonthenet.blogspot.com]

  • Fraser Syndrome

    […] or without cleft palate were observed less frequently than previously reported.[ncbi.nlm.nih.gov] Cognitive deficits and congenital heart disease are common. Genetics Fraser syndrome 1 is caused by homozygous or heterozygous mutations in the FRAS1 gene (4q21.21).[disorders.eyes.arizona.edu] Knoers & Albertien M. van Eerde Nature Reviews Nephrology (2016) Genetic link between renal birth defects and congenital heart disease Jovenal T.[doi.org]

  • Miller Dieker Syndrome

    palate, limb abnormalities and omphalocele.[ncbi.nlm.nih.gov] Prenatal ultrasonography findings in MDS are smooth gyral pattern, ventriculomegaly, large subarachnoid space, congenital heart disease and omphalocele [6] [7] .[ijcasereportsandimages.com] Additionally, congenital anomalies such as omphalocele and heart defects are also identified prenatally.[symptoma.com]

  • Otitis Media

    Cleft Palate – Serous otitis media is more common in the child with a cleft palate.[netwellness.org] […] antibiotics if: they have a serious health condition that makes them more vulnerable to complications, such as cystic fibrosis or congenital heart disease symptoms are showing[nhsinform.scot] Further, patients with craniofacial abnormalities (eg, Down syndrome, cri du chat syndrome, cleft lip and/or cleft palate, velocardiofacial syndrome [Shprintzen syndrome])[msdmanuals.com]

  • Terminal 4q Deletion Syndrome

    We delineate intervals with recurrent phenotypic overlap, particularly for cleft palate, congenital heart defect, intellectual disability, and autism spectrum disorder.[ncbi.nlm.nih.gov] In some individuals with Monosomy Distal 4q, congenital heart disease and/or respiratory difficulties associated with certain craniofacial malformations (e.g., Pierre-Robin[rarediseases.org] Other clinical features included atrial septal defect, patent ductus arteriosus, micrognathia, cleft palate, inner epicanthal folds and long philtrum.[ashg.org]

  • Apert Syndrome

    […] lip parent support group, cleft palate parent support group, cleft, lip, palate, advocate, insurance, birth, defect, cleft lip and palate, cleft lip and cleft palate, cleft[cleftadvocate.org] Abstract Apert syndrome (AS) is a rare autosomal dominant disorder characterised by craniosynostosis and limb malformations, and is associated with congenital heart disease[ncbi.nlm.nih.gov] Other abnormalities includes central nervous system anomalies, congenital heart diseases, cleft palate, and urogenital diseases.[ncbi.nlm.nih.gov]

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