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23 Possible Causes for Cardiomyopathy, Variable Malocclusions

  • Cri Du Chat Syndrome

    malocclusion, more commonly anterior open-bite.[] The main orofacial anomalies registered were mandibular microretrognathia, high palate but rarely cleft, variable malocclusion (frequently anterior open-bite), enamel hypoplasia[] RESULTS: The principal characteristics were skeletal class II malocclusion, caused by mandibular retrognathism, dental biprotrusion, and a small upper airway.[]

  • Microtia

    Facial asymmetry, malocclusion, facial nerve palsy, and macrostomia as well as thoracic deformities can also accompany MI.[] Disorders Cancer and Blood Disorders Cancer Predisposition Clinic Heart Cardiac Anesthesia Heart Cardiac Catheterization Heart Cardiac Surgery Heart Cardiology Clinic Heart Cardiomyopathy[] MI often presents as a mild form of GS and share the following characteristics: variable phenotypic expression, asymmetric facial anatomy, right side preponderance, male predilection[]

  • Kohlschütter-Tönz Syndrome

    […] in muscle fiber diameter Abnormal isoelectric focusing of serum transferrin Delayed myelination Poor suck Deep palmar crease Nail dysplasia Trigonocephaly Dental malocclusion[] 210900 Brittle cornea syndrome 1 ZNF469 229200 Butirilcholinesterase deficiency BCHE 177400 Canavan Disease ASPA 271900 Carbamoylphosphate synthetase I deficiency CPS1 237300 Cardiomyopathy[] […] onset Splenomegaly Lower limb hyperreflexia Apnea Peripheral neuropathy Feeding difficulties Upslanted palpebral fissure Hyperactivity Premature skin wrinkling Increased variability[]

  • Amelogenesis imperfecta Type 2A3

    Chediak-Higashi syndrome cleft lip-palate-ectodermal dysplasia syndrome Cockayne syndrome cold-induced sweating syndrome craniolenticulosutural dysplasia cystic fibrosis dilated cardiomyopathy[]

  • Renpenning Syndrome

    In puberty there is pronounced growth of testes. abnormal speech pattern, large ears, long face, high-arched palate, and malocclusion.[] Food and Drug Administration granted Priority Review to Pfizer for its application to market tafamidis, its treatment for transthyretin amyloid cardiomyopathy (ATTR-CM), a[] , dilated, with ataxia 610198 AR HUT, APA Cardiomyopathy, hypertrophic 600958 AR OOA, DGM Carnitine palmitoyl transferase I deficiency 255120 AR HUT Cartilage-hair hypoplasia[]

  • Amelo-Onycho-Hypohidrotic Syndrome

    Variable malocclusions were observed, and 1 affected individual also had anterior open bite. Teeth were sensitive to thermal and physical stimuli.[] - hypotonia - lactic acidosis Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency Cardiomyopathy with myopathy due to COX deficiency Cardioskeletal myopathy[] Class II or III malocclusion. Open bite. Facial bone formation Hypoplasia of the malar bones. Hypoplastic lateral aspects of orbits.[]

  • Congenital Velopharyngeal Incompetence

    Our findings qualify the variable relation between nasal obstruction and facial growth in line with Moss’s functional matrix theory, which stipulates that facial growth is[] […] complications: Encephalitis Hemiconvulsion- hemoplegia-epilepsy syndrome Chorea encephalopathy Neuropathy Frontal lobe seizures Neuralgic amytrophy • Myocarditis • Dilated cardiomyopathy[] The array of occlusal and cephalometric changes was similar in these animals and the investigated children, whose various malocclusions were also probably related to individual[]

  • Craniosynostosis Type 3

    High risk for Chiari malformation -Usually normal mental status Features of Saethre-Chotzen syndrome 1 / 50,000 AD inheritance TWIST gene mutation Characteristics: (Many - variable[] Mediterranean fever Familial medullary thyroid carcinoma Familial mitral valve prolapse Familial or sporadic hemiplegic migraine Familial paroxysmal ataxia Familial restrictive cardiomyopathy[] […] inheritance Mutations FGFR1 - 3 Features -Turribrachycephaly/ Kleeblattschadel -BROAD thumbs or great toes -Midface hypoplasia - BEAK nose -Mild cutaneous syndactyly -Class III malocclusion[]

  • Isolated Trigonocephaly

    There may associated FGFR3 mutation and phenotypic variability between generations is a common observation. Apert syndrome was described by Apert in 1906.[] […] atrioventricular orifice 【右房室弁閉鎖症】*right atrioventricular valve atresia 【鬱血】*congestion 【鬱血性肝硬変】*congestive cirrhosis 【鬱血性細気管支炎】*congestive bronchiolitis 【鬱血性心筋症】*congestive cardiomyopathy[] Apart from craniosynostosis this condition manifests maxillary hypoplasia, exorbitsm with hyperteleorism, and typeIII malocclusion. It has no obvious skeletal anomalies.[]

  • Kabuki Syndrome

    Kabuki syndrome is a rare autosomal dominant trait with variable clinical expression.[] Minor Features/ Signs and Symptoms Scoliosis or lateral deviation of the spine Cleft lip or cleft palate Cardiovascular problems such as atrial septal defects, hypertrophic cardiomyopathy[] Common dental manifestations of Kabuki syndrome are high-arched palate, micrognathia, malocclusion, microdontia, small dental arches, hypodontia, severe maxillary recession[]

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