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131 Possible Causes for Cerebellar Hypoplasia, Osteoporosis, Rheumatic Heart Disease

  • Ankylosing Spondylitis

    After AS diagnosis, a higher proportion of patients developed newly diagnosed cases of cardiovascular diseases, depression, osteoporosis, spinal fracture, IBD, psoriasis,[] It is an autoimmune disorder, an inflammatory arthritic disorder, a rheumatic disease, and one of the various spondylarthropathies.[] Clinical: Cerebral and cerebellar agyria-micropolygyria; cortical disorganization; glialmesodermal proliferation; neuronal heterotopias; hypoplasia of nerve tracts; hydrocephalus[]

  • Dyskeratosis Congenita

    Other findings include carious teeth, premature graying of hair, and osteoporosis. Approximately 50% of patients develop pancytopenia.[] An echocardiogram showed mitral and aortic valve thickening suggestive of rheumatic heart disease with mitral regurgitation.[] hypoplasia, severe immunodeficiency, enteropathy, and intrauterine growth retardation.[]

  • Reiter's Syndrome

    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[] Reiter syndrome is a systemic rheumatic disease, meaning that it can and does affect organs as well as the joints.[] Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential[]

  • Lutembacher Syndrome

    Alsing Syndrome Alstrom syndrome Alves Castelo dos Santos Syndrome Ameloonychohypohidrotic Syndrome Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis[] The most common cause of mitral stenosis is valvular heart disease or rheumatic heart disease.[] Forty-four out of 47 cases had rheumatic heart disease while one had endocardial cushion defect, one had Lutembacher's syndrome, and one had left atrial myxoma.[]

  • Lytic Bone Lesion

    Progressive focal bone destruction, including acroosteolysis and generalized osteoporosis.[] No association with transplant medications has been noted. [34] Congenital cyanotic congenital heart diseases, rheumatic diseases, and left ventricular tumors have been noted[] […] ataxia type 1 autosomal recessive cerebellar ataxia with mental retardation, see VLDLR-associated cerebellar hypoplasia autosomal recessive cerebellar hypoplasia with cerebral[]

  • Ehlers-Danlos Syndrome

    Read More hoop311 eds-and-osteoporosis-nficj1 200212 I am 54 and have been dx with osteoporosis in both hips and lumbar spine.[] Miller, W.S. jacoby Ehlers-DAnlos syndrome with a sinus of Valsalva aneurysm and aortic insuficiency Sinalating Rheumatic Heart Disease. Am. J.[] As opposed to the less pronounced tonsillar herniation seen with Chiari I, there is a larger cerebellar vermian displacement.[]

  • Autosomal Dominant Dyskeratosis Congenita 2

    It is variably accompanied by premature greying, aplastic anaemia, low platelets, osteoporosis, pulmonary fibrosis and liver fibrosis.[] An echocardiogram showed mitral and aortic valve thickening suggestive of rheumatic heart disease with mitral regurgitation.[] hypoplasia.[]

  • Spondylo-Ocular Syndrome

    The segregation of flanking marker alleles of three collagen genes and the interval for osteoporosis-pseudoglioma syndrome were analyzed.[] Exclusion Criteria of SPTS The patients who have above symptoms while suffering from hypertension, coronary heart disease, arrhythmia, rheumatic heart disease, myocarditis[] hypoplasia Babinski sign Encephalopathy Dystonia Ventriculomegaly Anemia Global developmental delay Homonymous hemianopia Impaired distal vibration sensation Sensory ataxic[]

  • Polyarthritis

    Bisphosphonates are the mainstay treatment for postmenopausal osteoporosis.[] RF and its most serious complication, rheumatic heart disease (RHD), are believed to result from an autoimmune response; however, the exact pathogenesis remains unclear. 2[] Gillespie syndrome, an autosomal recessive form of aniridia, is associated with cerebellar ataxia and mental retardation seen in 2% of patients with aniridia.[]

  • Sneddon's Syndrome

    Seite 193 - Myeloma Osteoporosis and Osteopenia Ovarian Cancer, Second Edition Overactive Bladder and Urinary Incontinence Pancreatic Cancer Panic Disorder Parkinson Disease[] In some patients, rheumatic heart disease is a possible causal association.[] […] due to TUBB3 mutation Cluster headache Microcephaly autosomal dominant Spinocerebellar ataxia Sneddon syndrome Cerebellar hypoplasia with endosteal sclerosis Dyskeratosis[]

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