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1,776 Possible Causes for Cutaneous Syndactyly of Digits, Hyperostosis, Narrowing of Medullary Canal

  • Van Buchem Disease

    Prevention - Hyperostosis corticalis generalisata Not supplied. Diagnosis - Hyperostosis corticalis generalisata Not supplied.[checkorphan.org] In about 75 % there is asymmetric partial or complete cutaneous syndactyly of the index and middle fingers.[slideheaven.com] […] of the medullary canal.[ncbi.nlm.nih.gov]

  • Sclerosteosis Type 2

    […] 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] Alternative names BEER CDD Cortical hyperostosis with syndactyly see all Function Negative regulator of bone growth.[abcam.com]

  • Camurati-Engelmann Syndrome

    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] Certain bone regions (specifically, the endosteal and periosteal surfaces) become abnormally thickened and hardened, which in turn narrows the medullary canal.[encyclopedia.com] […] of the medullary canals.[synapse.koreamed.org]

    Missing: Cutaneous Syndactyly of Digits
  • Craniodiaphyseal Dysplasia

    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] In about 75 % there is asymmetric partial or complete cutaneous syndactyly of the index and middle fingers.[slideheaven.com] […] 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]

  • Melorheostosis

    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] Radiographs demonstrated endosteal hyperostosis, which were consistent with a mixed picture of melorheostosis and osteopoikilois.[ncbi.nlm.nih.gov]

    Missing: Cutaneous Syndactyly of Digits
  • Osteosclerosis

    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] medullary canals.[dx.doi.org] "Osteosclerosis, hyperostosis, and related disorders". United States. doi:.[osti.gov]

    Missing: Cutaneous Syndactyly of Digits
  • Lenz-Majewski Syndrome

    The life-threatening complication was related to progressive craniovertebral hyperostosis that rapidly exacerbated during early childhood.[ncbi.nlm.nih.gov] Delayed closure of fontanelle, proximal symphalangism, short digits, partial syndactyly, prominent cutaneous veins, loose and wrinkled atrophic skin of hands, skin hypoplasia[accessanesthesiology.mhmedical.com] Patients have multiple radiographic abnormalities due to progressive generalized hyperostosis that affects the cranium, vertebrae, and diaphyses of tubular bones, leading[malacards.org]

    Missing: Narrowing of Medullary Canal
  • Schwartz-Lelek Syndrome

    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] OR WITHOUT ANOSMIA; HH17 Low match CRANIOMETAPHYSEAL DYSPLASIA Craniometaphyseal dysplasia (CMD) is a very rare genetic bone disease characterized by progressive diffuse hyperostosis[mendelian.co]

    Missing: Cutaneous Syndactyly of Digits
  • Hereditary Hyperphosphatasia

    Synonyms of Hereditary Hyperphosphatasia Chronic Congenital Idiopathic Hyperphosphatasemia Familial Idiopathic Hyperphosphatasia Familial Osteoectasia Hyperostosis Corticalis[hekim.org] In about 75 % there is asymmetric partial or complete cutaneous syndactyly of the index and middle fingers.[slideheaven.com] Synonyms JPG chronic congenital idiopathic hyperphosphatasemia familial idiopathic hyperphosphatasia familial osteoectasia hyperostosis corticalis deformans juvenilis juvenile[healthmedicinet.com]

    Missing: Narrowing of Medullary Canal
  • Acquired Osteosclerosis

    Radiology 119:55–9 CrossRef Google Scholar Resnick D, Shapiro RF, Wiesner KB et al (1978c) Diffuse idiopathic skeIetaI hyperostosis (DISH) (ankylosing hyperostosis of Forestier[link.springer.com] This disease of bone tissue, which is manifested by an increase in the density of bone structure, as well as narrowing of the medullary canal in the volume.[acikgunluk.net] [DISH] ( ICD-10-CM Diagnosis Code M48.1 Ankylosing hyperostosis [Forestier] 2016 2017 2018 2019 Non-Billable/Non-Specific Code Applicable To Diffuse idiopathic skeletal hyperostosis[icd10data.com]

    Missing: Cutaneous Syndactyly of Digits

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