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1,268 Possible Causes for Hemochromatosis, Scoliosis

  • Thalassemia

    Almost a third of the cases had kyphosis and/or scoliosis, and chest wall deformity was seen in 10 cases.[] Abstract The authors present a unique case of torsades de pointes in a β-thalassemia patient with early iron overload in the absence of any structural abnormalities as seen in hemochromatosis[] […] cut appearance of the skull secondary to extramedullary hematopoiesis in the skull Treatment β-thalassemia major frequent transfusions required can cause iron overload and hemochromatosis[]

  • Hemochromatosis

    […] fraction of 15%, severe pulmonary hypertension, mitral insufficiency, a history of ventricular tachycardia, cirrhosis, obstructive sleep apnea, gestational diabetes, and severe scoliosis[] Hemochromatosis usually occurs in men above the age of 50 years.[] Epub 2015 Jul 8. bronze diabetes bronzed cirrhosis familial hemochromatosis genetic hemochromatosis haemochromatosis HC hemochromatosis hereditary haemochromatosis HH HLAH[]

  • Hypogonadism

    […] skills, facial abnormalities (eg, a narrow bitemporal dimension, almond-shaped eyes, a mouth with thin upper lips and down-turned corners), and skeletal abnormalities (eg, scoliosis[] Ann Intern Med 101 : 629 – 632 8 1983 The endocrine manifestations of hemochromatosis. Am J Med Sci 285 : 7 – 13 9 1980 The GnRH test in idiopathic hemochromatosis.[] HEMOCHROMATOSIS Hemochromatosis presents with combined secondary hypogonadism Occurs when serum ferritin levels exceed 1500 micro/dl.[]

  • Friedreich Ataxia

    scoliosis due to Friedreichs ataxia Lumbar neuromuscular scoliosis due to Friedreich's ataxia Lumbar scoliosis due to Friedreichs ataxia Lumbosacral neuromuscular scoliosis[] One patient with homozygous trinucleotide repeat expansions and comorbid hemochromatosis had more severe FRDA symptoms than his sibling without hemochromatosis. p.R165P patients[] This restricted localization of the metal contrasts with the diffuse cardiac Fe overload in hemochromatosis and transfusion siderosis.[]

  • Osteogenesis Imperfecta

    Scoliosis can be divided into the three major types: Idiopathic Scoliosis The cause has not been discovered so far.[] "Hereditary hemochromatosis". Genetics Home Reference. Retrieved 2018-01-24. a b National Library of Medicine, Genetics Home Reference.[] […] present as a minor component Primary OA: most common, insidious onset, no initiating factor, oligoarticular Secondary OA: 5% of cases, young age, history of trauma, DM, hemochromatosis[]

  • Jarcho-Levin Syndrome

    If scoliosis is significant surgical intervention is given. Secondary complications must be prevented.[] Detection of mutations C282Y, H63D and S65C in the HFE gene Hemochromatosis Sanger Sequencing of the HFE gene Hemochromatosis type 3 Sanger Sequencing of the TFR2 gene Hemolytic[] It is also emphasized that even when there is moderate scoliosis associated costal deformities may cause anti-cosmetic thoracic gibbosity.[]

  • Multiple Sclerosis

    He had a bifid uvula, bilaterally duplicated thumbs and scoliosis. Additionally, he had hypertelorism, a wide forehead and flattening of mid-face.[] Disease Type I Haemophilus Influenzae Infection Hantavirus Pulmonary Syndrome Heart Transplantation Helicobacter Pylori Infection Hematopoietic Stem Cell Transplantation Hemochromatosis[] Homozygous hPDGF-A tg mice exhibit deformity of the spinal cord (scoliosis) and die within the first few postnatal weeks.[]

  • Turner Syndrome

    Scoliosis The incidence of scoliosis in TS patients was 0.69%, compared with 0.39% among non-TS patients.[] Rare causes of adult GHD include diseases such as sarcoidosis, tuberculosis, histiocytosis, and hemochromatosis (iron overload).[] […] thyroiditis (25.2%), inflammatory bowel disease (1.8%), congenital cardiovascular anomaly (11.8%), urinary tract malformation (11.8%), low bone mineral density (BMD) (42.9%), scoliosis[]

  • Sideroblastic Anemia

    There was no scoliosis, pes cavus, or muscle wasting in any of the families.[] Idiopathic hemochromatosis is a hereditary disease that is associated with human leucocytic antigens A3, B7, and B14.[] A severely anemic 3-year-old girl with refractory sideroblastic anemia and fulminant, fatal hemochromatosis is described.[]

  • Torticollis

    The manifestations of the WS in this patient are severe: she has torticollis, and an extremely severe scoliosis.[] Recognized causes of calcification in adult intervertebral disc such as hyperparathyroidism, hemochromatosis and ochronosis have not been implicated in children.[] Late-onset, asymptomatic thoracic scoliosis (8-13 degrees) in CMT also described. 7 Hip dysplasia: 2 to 20% incidence versus 2% in general population. 1 Motor developmental[]

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