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12 Possible Causes for Bell's Palsy, Muscular Atrophy, Narrowing of Medullary Canal

  • Camurati-Engelmann Syndrome

    Certain bone regions (specifically, the endosteal and periosteal surfaces) become abnormally thickened and hardened, which in turn narrows the medullary canal.[] […] dystrophy type 2A Craniofacial deafness hand syndrome Myoclonus hereditary progressive distal muscular atrophy Steinfeld syndrome Cardiomyopathy dilated with woolly hair[] ’s palsy. 16 , 179 Those with a more indolent course may have progressive venous congestion associated with foraminal overgrowth, resulting in edema and subsequent arterial[]

  • Pyle's Disease

    Progressive muscular atrophy and decreased subcutaneous fat in the limbs also can occur. Easy fatigability is a symptom that has been described in 44%.[] […] ganglia disease syndrome Infantile systemic hyalinosis Infantile-onset X-linked spinal muscular atrophy Intellectual disability, Birk-Barel type Intellectual disability,[] Initially begins in the diaphyses and it extends to the metaphyses, sparing the epiphyses. 16,20,21 As a consequence it can be seen a narrowing of the medullary canal with[]

  • Lower Motor Neuron Syndrome with Late-Adult Onset

    muscular atrophy, but have different genetic causes.[] This causes Bell palsy , an abrupt weakness of all the facial muscles on one side of the face that is often accompanied by pain around the ear, unusual loudness of sounds[] The spinal cord terminates in the conus medullaris (L1), which then become lumbosacral roots (cauda equina) descending through the lumbar spinal canal.[]

  • Schwartz-Lelek Syndrome

    Spinal muscular atrophy with congenital bone fractures Spinal muscular atrophy with lower extremity predominance 1 Spinal muscular atrophy with lower extremity predominance[] palsy Bellini Chiumello Rimoldi Syndrome Ben Ari Shuper Mimouni Syndrome Bent Bone Dysplasia Syndrome Berk-Tabatznik Syndrome Bernard-Soulier syndrome Bhaskar Jagannathan[] , sclerotic medullary canal Type III: Anterior bowig with a cystic lesion or prefracture Type IV: Anterior bowing with a frank fracture and pseudarthrosis usually involving[]

  • Autosomal Dominant Osteopetrosis Type 1

    The long bones were uniformly dense with very narrow medullary canals. The lumbar vertebrae were also dense with degenerative changes present.[] 2018 2017 2016 2015 2014 2013 2011 2010 2009 2008 2007 2006 2005 2004 2018 Eva Janzen: Novel Modifiers for Inherited Neurogenerative Disorders - Spinal Muscular Atrophy and[] atrophy without contractures Autosomal dominant nonsyndromic intellectual deficit Autosomal dominant spastic paraplegia type 13 Baraitser-Winter syndrome Catecholaminergic[]

  • Amaurosis-Hypertrichosis Syndrome

    The bone involvement is complex with narrow thorax, broad ribs, platyspondyly, hypoplastic idiopathic branches, small obturator foramen, bilateral coxa valga, large medullary[] atrophy Adult syndrome Ae-Ah Aerophobia Afibrinogenemia Aganglionosis, total intestinal Aggressive fibromatosis Agnathia holoprosencephaly situs inversus Agnosia, primary[] ’s Palsy Bile Duct, Dilated Bipolar Disorder Bites And Stings, Arachnids Bites And Stings, Insect Bites, Snake Bladder Cancer Blastomycosis Bleeding, Lower GI Bleeding, Lower[]

  • Quadriplegia

    atrophy.[] Other causes of paralysis include Nerve diseases such as amyotrophic lateral sclerosis Autoimmune diseases such as Guillain-Barre syndrome Bell's palsy, which affects muscles[] The MR images show the spondyloarthrotic changes and a narrow canal and the secondary myelopathy, with signal changes in medullary area [Images courtesy of the Neuroradiology[]

  • Hypertrichotic Osteochondrodysplasia

    atrophy , see spinal muscular atrophy with progressive myoclonic epilepsy hereditary myopathy with early respiratory failure hereditary myopathy with lactic acidosis , see[] palsy 【顔面肉芽腫】*facial granuloma *granuloma faciale[L] 【顔面変形症】*prosopodysmorphia 【顔面裂】【顔裂】*facial cleft *prosoposchisis 【義歯性口内炎】*denture stomatitis 【義歯性線維腫】*denture fibroma[] Thickened calvarium, narrow thorax, wide ribs, flattened or ovoid vertebral bodies, coxa valga, osteopenia, enlarged medullary canals, and metaphyseal widening of long bones[]

  • Sclerosteosis Type 2

    […] of medullary canal; erlenmeyer flask defect of the bone; clubfoot (genu varus and valgus deformities); relative muscle weakness, especially in pelvic girdle; atrophic muscle[] […] respiratory failure Musk retinal disease Chat schizophrenia Chrna7 sclerosteosis Lrp4 sclerosteosis 2 Lrp4 sleep disorder Chrna4 , Chrnb2 Spina Bifida Cystica Chrna7 spinal muscular[] Acute, repeated attacks of facial palsy, similar to Bell's palsy, are usually the first symptoms in both conditions.[]

  • Osteopetrosis

    medullary canals.[] Treatment of facial palsy Eye protection Specific treatment : Bell’s palsy ; steroids and decompression. Ramsay Huntsyndrom ; acyclovir. Trauma ; exploration and repair.[] Symptoms of the intermediate type of osteopetrosis may also include gradual deterioration of the nerves of the eyes (optic atrophy), loss of vision, muscular weakness, and[]

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