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58 Possible Causes for Cerebellar Hypoplasia, Osteoporosis, Spondylarthropathy

  • Ankylosing Spondylitis

    Pathology of the spondylarthropathies. In: Calin A, ed. Spondylarthropathies. Orlando: Grune & Stratton; 1984:43–68.[doi.org] After AS diagnosis, a higher proportion of patients developed newly diagnosed cases of cardiovascular diseases, depression, osteoporosis, spinal fracture, IBD, psoriasis,[ncbi.nlm.nih.gov] Clinical: Cerebral and cerebellar agyria-micropolygyria; cortical disorganization; glialmesodermal proliferation; neuronal heterotopias; hypoplasia of nerve tracts; hydrocephalus[dentisty.org]

  • Lumbar Spondylosis

    Assessment of the efficacy of sacroiliac corticosteroid injections in spondylarthropathies: a double-blind study.[ncbi.nlm.nih.gov] […] started a large-scale population-based cohort study entitled research on osteoarthritis/osteoporosis against disability (ROAD) in 2005.[ncbi.nlm.nih.gov] Angiography showed two extracranial right vertebral artery (VA) stenoses, left VA hypoplasia, absence of left PICA and a dominant right PICA.[doi.org]

  • Reiter's Syndrome

    These 2 cases illustrate the pathophysiologic hypothesis of Reiter's syndrome, emphasizing the role of environmental triggering factors and the relationship between spondylarthropathies[ncbi.nlm.nih.gov] It can have a very similar appearance to psoriatic arthritis with the classic features of ill-defined erosions, enthesopathy, bone proliferation, early juxta-articular osteoporosis[radiopaedia.org] Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential[rarediseases.org]

  • Parastremmatic Dwarfism

    Spondylarthropathy Spondylitis Spondylo Spondylo camptodactyly syndrome Spondylo costal dysostosis dandy walker Spondylocarpotarsal synostosis Spondylocostal dysplasia dominant[sosu.us] […] inheritance - Bowed diaphysis / diaphyses / long bones - Epiphyseal anomaly - Genu valgum - Kyphosis - Lack / delayed ossification of spine / vertebrae - Metaphyseal anomaly - Osteoporosis[csbg.cnb.csic.es] hypoplasia and distinctive facial appearance ORC1 Meier-Gorlin syndrome (Ear-patella-short stature syndrome) ORC4 Meier-Gorlin syndrome (Ear-patella-short stature syndrome[genda.com.ar]

  • Singleton Merten Syndrome

    […] autosomal recessive Split hand split foot mandibular hypoplasia Split hand split foot nystagmus Split hand urinary anomalies spina bifida Split hand/foot malformation X-linked Spondylarthropathy[personalizedcause.com] There are no life-threatening causes of osteoporosis . However, complications resulting from untreated osteoporosis are common.[wikidoc.org] hypoplasia X-linked recessive inheritance Hypertonia Wide nose Hydrocephalus Brachydactyly High palate Cataract Palmoplantar cutis gyrata Abnormality of primary teeth Slender[mendelian.co]

  • Spondyloepimetaphyseal Dysplasia Type SPONASTRIME

    Spondylarthropathy Spondylitis Spondylo Spondylo camptodactyly syndrome Spondylo costal dysostosis dandy walker Spondylocarpotarsal synostosis Spondylocostal dysplasia dominant[sosu.us] There are no life-threatening causes of osteoporosis . However, complications resulting from untreated osteoporosis are common.[wikidoc.org] hypoplasia Epiphyseal dysplasia Familial expansile osteolysis Finding of arrangement of skeletal muscle Hereditary acrosteolysis Hypochondrogenesis Hypochondroplasia Idiopathic[emedcodes.com]

  • Spondylometaphyseal Dysplasia Type Kozlowski 

    Spondylarthropathy Spondylitis Spondylo Spondylo camptodactyly syndrome Spondylo costal dysostosis dandy walker Spondylocarpotarsal synostosis Spondylocostal dysplasia dominant[wikidoc.org] , Dian Jing , Jin Hao , Ge Tang , Pu Yang & Zhihe Zhao Calcified Tissue International (2018) Extracellular Matrix and Developing Growth Plate Johanna Myllyharju Current Osteoporosis[nature.com] hypoplasia.[ncbi.nlm.nih.gov]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    […] autosomal recessive Split hand split foot mandibular hypoplasia Split hand split foot nystagmus Split hand urinary anomalies spina bifida Split hand/foot malformation X-linked Spondylarthropathy[personalizedcause.com] […] primary B-cell expansion with NFKB and T-cell anergy Bare lymphocyte syndrome Beare-Stevenson cutis gyrata syndrome Bent bone dysplasia syndrome Bone mineral density QTL18, osteoporosis[qlinics.com] hypoplasia Microcephaly Microcephaly 1 primary autosomal recessive Microcephaly 5 primary autosomal recessive Microcephaly 6 primary autosomal recessive Microcephaly 7 primary[agdx.portal.cartagenia.com]

  • Polyarthritis

    Late onset peripheral spondylarthropathy Pitting oedema is a feature of late onset peripheral spondylarthropathy as described by Dubost et al , 29 but unlike RS3PE, it affects[ard.bmj.com] Bisphosphonates are the mainstay treatment for postmenopausal osteoporosis.[ncbi.nlm.nih.gov] Gillespie syndrome, an autosomal recessive form of aniridia, is associated with cerebellar ataxia and mental retardation seen in 2% of patients with aniridia.[eyewiki.aao.org]

  • Patterson Pseudoleprechaunism Syndrome

    Spondylarthropathy Spondylitis Spondylo Spondylo camptodactyly syndrome Spondylo costal dysostosis dandy walker Spondylocarpotarsal synostosis Spondylocostal dysplasia dominant[sosu.us] Congenital Cutis Laxa and Osteoporosis. Am J Dis Child. 1983;137(5):452–454. doi:10.1001/archpedi.1983.02140310034008 Download citation file: 2019 New![jamanetwork.com] HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE X-linked intellectual deficit-cerebellar hypoplasia, also known as OPHN1 syndrome, is a rare syndromic form of cerebellar dysgenesis[mendelian.co]

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