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55 Possible Causes for Hyperostosis, 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.[encyclopedia.com] […] dystrophy type 2A Craniofacial deafness hand syndrome Myoclonus hereditary progressive distal muscular atrophy Steinfeld syndrome Cardiomyopathy dilated with woolly hair[checkrare.com] However, the skull hyperostosis is progressive, and cranial nerve compression often recurs. Corticosteroids may delay skull hyperostosis and cranial nerve impingement.[ncbi.nlm.nih.gov]

  • Cervical Spondylosis

    Conditions excluded from this SOP Ankylosing spondylitis* Diffuse Idiopathic Skeletal Hyperostosis (DISH) # Facet joint dysfunction # Isolated bulging of a disc – A disc bulge[clik.dva.gov.au] […] of the medullary canal [14].[termedia.pl] 721.41 to ICD-10-CM 721.42 Spondylosis with myelopathy, lumbar region convert 721.42 to ICD-10-CM 721.5 Kissing spine convert 721.5 to ICD-10-CM 721.6 Ankylosing vertebral hyperostosis[icd9data.com]

  • Melorheostosis

    Clinically, patients affected may have pain and stiffness of the involved bones, contractures when the osseous abnormality involves a joint, muscular atrophy and overlying[iofbonehealth.org] Melorheostosis Leri’s Disease, Flowing Periosteal Hyperostosis One of a group of sclerosing bone disorders Rare Cause is unknown Produces thickening of the endosteum and periosteum[learningradiology.com] The lesions of the cortex are progressive and may result in narrowing of the medullary canal and stenosis of an adjacent lumen, foramen, or of the spinal canal .[boneandspine.com]

  • 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[en.wikipedia.org] Physical Fitness) Cleanses & Detoxifying Katz Syndrome “Katz Syndrome” In our body, the dis-order, Katz Syndrome is the allopathic name of a shortness of stature , cranial hyperostosis[wellnessadvocate.com] , 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[flinders.edu.au]

  • Craniodiaphyseal Dysplasia

    […] dystrophy type 2A Craniofacial deafness hand syndrome Myoclonus hereditary progressive distal muscular atrophy Steinfeld syndrome Cardiomyopathy dilated with woolly hair[checkrare.com] Imbalance will lead to conditions such as osteoporosis or hyperostosis. Osteoblasts build bone, becoming embedded in bone matrix as mature osteocytes.[ncbi.nlm.nih.gov] […] of medullary canal; erlenmeyer flask defect of the bone; clubfoot (genu varus and valgus deformities); relative muscle weakness, especially in pelvic girdle; atrophic muscle[encyclopedia.com]

  • Osteosclerosis

    There may also be associated muscular atrophy and overlying skin changes.[dx.doi.org] Radiographically, affected members exhibit generalized, symmetrically diffuse endosteal hyperostosis of the long bones and skull with narrow medullary cavities and loss of[ncbi.nlm.nih.gov] "Osteosclerosis, hyperostosis, and related disorders". United States. doi:.[osti.gov]

  • Sclerosteosis Type 2

    […] respiratory failure Musk retinal disease Chat schizophrenia Chrna7 sclerosteosis Lrp4 sclerosteosis 2 Lrp4 sleep disorder Chrna4 , Chrnb2 Spina Bifida Cystica Chrna7 spinal muscular[rgd.mcw.edu] […] hypertelorism, wide and dense clavicles-ribs, sclerotic calvarium, enlarged and sclerotic mandible, sclerotic vertebral end plates and pedicles, sclerotic pelvic bones, cortical hyperostosis[iofbonehealth.org] […] of medullary canal; erlenmeyer flask defect of the bone; clubfoot (genu varus and valgus deformities); relative muscle weakness, especially in pelvic girdle; atrophic muscle[encyclopedia.com]

  • Frontometaphyseal Dysplasia

    atrophy without contractures Autosomal dominant macrothrombocytopenia Autosomal dominant nonsyndromic intellectual deficit Autosomal recessive centronuclear myopathy Autosomal[csbg.cnb.csic.es] This condition is characterized by hyperostosis of the skull and prominence of the supraorbital ridges; long bones have flared metaphyses.[ncbi.nlm.nih.gov] […] of medullary canal; erlenmeyer flask defect of the bone; clubfoot (genu varus and valgus deformities); relative muscle weakness, especially in pelvic girdle; atrophic muscle[encyclopedia.com]

  • Metaphyseal Chondrodysplasia, Spahr Type

    1719 myotonia permanens 1720 mycoplasmal pneumonia 1721 acute interstitial pneumonia 1722 cervical dystonia 1723 bifid uvula 1724 acute myocarditis 1725 juvenile spinal muscular[pediascape.org] Ehlers-Danlos syndrome, spondylocheirodysplastic type Ehlers-Danlos/osteogenesis imperfecta syndrome Eiken syndrome Ellis Van Creveld syndrome Enchondromatosis Endosteal hyperostosis[se-atlas.de] , 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[flinders.edu.au]

  • Kenny-Caffey Syndrome Type 1

    (PMID: 8706133) Tian G … Cowan NJ (Cell 1996) 2 3 4 60 TBCE Mutations Cause Early-Onset Progressive Encephalopathy with Distal Spinal Muscular Atrophy.[genecards.org] Camurati-Engelmann Syndrome : A musculoskeletal syndrome leading to enhanced bone formation, hyperostosis and sclerosis of the diaphyses of the long bones.[accessanesthesiology.mhmedical.com] 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[elsevier.es]

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