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65 Possible Causes for High Arched Palate, High Foot Arch, Marfan Syndrome

  • Marfan Syndrome

    Reviewed February 2008 What is Marfan syndrome? Marfan syndrome is a disorder of the connective tissue.[] arch palate, crowded teeth RESP: emphysema, spontaneous pneumothorax, pectus excavatum, tracheomalacia, OSA, kyphoscoliosis CVS: dilated ascending aorta, dissecting aneurysms[] Physical Appearance/Skeletal Tall and slender, a narrow face, deep-set eyes, receding chin, down slanted eyes, high arched palate with crowded teeth Arm span length greater[]

  • Hypermobility Syndrome

    […] distinct from, the Marfan and Ehlers-Danlos syndromes.[] They frequently have tall parents usually the father and often have a high arched palate. They often are excellent gymnasts and are good at ballet.[] Footwear There’s a wide variation in the shape of the foot in people who are hypermobile. Most tend to have flat feet but a few have a high-arched foot.[]

  • Tel Hashomer Camptodactyly Syndrome

    DW (l99l) Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes. ‎[] Features compatible with skeletal muscle and/ or connective tissue involvement include high-arched palate, hypoplastic and hypotonic muscles, scapulae ala-tae, thoracic scoliosis[] * Dislocated joints * Club foot * Webbed fingers * Short stature * Curved spine * Overlapping toes * Narrow rib cage * Narrow hips * High arched palate * Prominent forehead[]

  • Mohr Syndrome

    Syndrome Digitised copy available UGC155/3/3/60 MD, Muscular dystrophy UGC155/3/3/61 MI, Milroy's Disease Digitised copy available UGC155/3/3/62 MT, 'Mt a' antigen Digitised[] It features oral deformities such as a cleft or high-arched palate, cleft lip, tongue nodules, and absent teeth.[] Mohr-claussen oral-facial digital syndrome OFDS typeII.J Pak Med Assoc 2009:59:486-8 [PubMed] [Free Full Text] Photograph 1 : showing high arch palate and absent uvula Photograph[]

  • Cap Myopathy

    Hypertrophic cardiomyopathy 7, 2 Nemaline myopathy 4, 5 Tropomyosin Hypertrophic cardiomyopathy 3 Nemaline myopathy 1 Titin Hypertrophic cardiomyopathy 9 Other Fibrillin Marfan[] They presented generalized hypotrophy and mild muscle weakness, elongated face, high arched palate, micrognathia, scoliosis and respiratory involvement.[] His first symptom was foot drop at the age of three, followed by distal muscle atrophy, slight hypomimia, high-arched palate, and weakness of the neck and elbow flexors, hands[]

  • Mobius Syndrome

    […] involving limbs Q87.3 Congenital malformation syndromes involving early overgrowth Q87.4 Marfan's syndrome Q87.41 Marfan's syndrome with cardiovascular manifestations Q87.410[] RESULTS: All patients presented micrognathia, lack of lip seal, high arched palate and weak soft palate.[] Other associated problems include club foot (approximately 30%), hand and upper limb deformities, Poland’s anomaly (approximately 15%) and high arched palate.[]

  • Schwartz-Jampel Syndrome

    He has always had an enlarged aortic root –another symptom of Marfan syndrome as well–and this is monitored by yearly echocardiograms.[] The children display facial dysmorphism (a small forehead, a flat base of the nose, a receding chin, an irregular order of the teeth, low-set ears, a high-arched palate, low[] The child had a short neck, blepharophimosis, flattened face, hypertrichosis of the eyelids, prominent eyebrows, high arched palate, low set ears, micrognathia, short stature[]

  • Craniofrontonasal Dysplasia

    症候群:Marfan syndrome O-2 Beals症候群:Beals syndrome O-3 Ehlers-Danlos症候群:Ehlers-Danlos syndrome O-4 骨形成不全症候群:osteogenesis imperfecta syndrome O-5 進行性化骨性線維異形成症:fibrodysplasia ossificans[] Autopsy of the aborted male foetus showed the following features: High arched palate, a sloping forehead, flattened nose and receding chin, multiple joint contractures, particularly[] arched palate, orbital dystopia, low implant of the breasts with asymmetric nipples and volume, webbed neck, hand or foot abnormalities such as clinodactyly (most common[]

  • Klinefelter Syndrome

    , Marfan syndrome Treatment Medical management testosterone replacement may deepen voice, increase muscle growth, and enhance sexual development may be helpful in assisting[] ., extra folds of skin), small jaws, and high arched palates. They generally lack prominent female secondary sexual characteristics.[] The differential diagnosis for KS can include fragile X syndrome, Kallmann syndrome, and Marfan syndrome.[]

  • Multicore Myopathy

    Pages M, Echenne B, Pages A-M, Dimeglio A, Sires A: Multi-core disease and Marfans syndrome: a case report. Eur Neurol1985;24:170175.15.[] arched palate * Poor infant feeding * Breathing problems * Delayed motor development * Difficulty running in childhood * Wasting of neck muscles * Wasting of shoulder girdle[] […] of the foot (flatfoot or pes panus), and an abnormally high arch of the foot (pes cavus).[]

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