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661 Possible Causes for Bifid Uvula

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  • Neuhauser Syndrome

    .: Megalocornea-mental retardation syndrome: another case associated with cerebral cortical atrophy and bifid uvula. Genet. Counsel., 2004, 15, 477-480. 8.[]

  • Stickler Syndrome Type 2

    uvula 0000193 Depressed nasal bridge Depressed bridge of nose Flat bridge of nose Flat nasal bridge Flat, nasal bridge Flattened nasal bridge Low nasal bridge Low nasal root[] uvula cleft hard palate micrognathia Robin sequence : micrognathia, cleft palate, glossoptosis Audiologic sensorineural or conductive hearing loss hypermobile middle ear[] In Family 6, none of the three examined had palate abnormalities, and in Family 7, one of five had a cleft palate and one of five had a bifid uvula.[]

  • Limb-Mammary Syndrome

    uvula.[] uvula, hypodontia was reported.[] Affiliated tissues include skin , bone and eye , and related phenotypes are cleft palate and bifid uvula UniProtKB/Swiss-Prot : 75 Limb-mammary syndrome: Characterized by[]

  • Brachyphalangy Polydactyly and Tibial Aplasia/Hypoplasia

    Bifid uvula may also be present.[] As defined by Loeys et al. (2006) , the disorder is characterized by the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate.[] uvula Bruising susceptibility Arachnodactyly Facial asymmetry Joint hyperflexibility Dolichocephaly Broad forehead Skeletal dysplasia Disproportionate tall stature Striae[]

  • Familial Isolated Trichomegaly

    uvula - Complete / partial microdontia - Conductive deafness / hearing loss - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - Dilated[] unerupted / dental ankylosis - Anodontia / oligodontia / hypodontia - Blue sclerae - Cardiac septal defect - Cleft palate without cleft lip / submucosal cleft palate / bifid[]

  • Aortic Aneurysm and Dissection

    uvula or cleft palate.[] uvula; translucent, easily bruised skin; or absence of ectopia lentis).[] […] in the transforming growth factor receptor Type I or II genes and is characterized by the triad of arterial tortuousity and aneurysms, hypertelorism (wide-set eyes), and bifid[]

  • High Myopia-Sensorineural Deafness Syndrome

    There was a small submucus cleft palate with bifid uvula ( Fig. 2 ). The child weighed 13 kilograms and was 102 cm in height, both parameters below 3rd percentile.[] This may also lead to ear infections High arched palate Bifid uvula Micrognathia (the lower jaw is shorter than normal) These problems may lead to difficulties with speech[] uvula).[]

  • Auriculocondylar Syndrome 3

    […] to: « Auriculocondylar syndrome Symptoms of Auriculocondylar syndrome type 3 Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of head or neck Bifid[] Affiliated tissues include bone , and related phenotypes are glossoptosis and bifid uvula UniProtKB/Swiss-Prot : 75 Auriculocondylar syndrome 3: A craniofacial malformation[] Auriculocondylar Syndrome 3 Synonyms - Classification bone, developmental, genetic, otorhinolaryngological, surgical maxillo-facial Phenotypes Autosomal recessive inheritance ; Bifid[]

  • Tenorio Syndrome

    Other systemic features include cleft palate, bifid uvula, mitral valve disease, skeletal overgrowth, cervical spine instability, and clubfoot deformity; however, not all[] uvula Blue sclerae Tall stature Mitral regurgitation Joint contracture of the hand Exotropia Osteoarthritis Aortic aneurysm Autoimmunity Ectopia lentis Cerebral hemorrhage[] Frontal balding Ascending aortic dissection Patent foramen ovale Smooth philtrum Abnormality of the foot Long face Arachnodactyly Joint hypermobility Bruising susceptibility Bifid[]

  • Syndromic Moyamoya Disease

    The disease is characterized by the triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate and is caused by heterozygous mutations in the[]

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