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13 Possible Causes for Hematomyelia, Hereditary Hemorrhagic Telangiectasia, Vein Disorder

  • Arteriovenous Malformation

    Arteriovenous malformation (AVM) is a vascular disorder in which arteries and veins are connected directly rather than through capillaries.[] Hereditary hemorrhagic telangiectasia (HHT) The natural history of HHT is not well understood.[] Vascular disorders of the spine Vascular disorders of the spine are a rare type of disease in which there is an abnormal short-circuit between arteries and veins occurring[]

  • Familial Isolated Congenital Asplenia

    […] atresia or stenosis Congenital tracheomalacia Congenital vitamin K-dependent coagulation factors deficiency Connective tissue disorder due to lysyl hydroxylase-3 deficiency[] […] polycythemia ( 赤血球増加症) (脊) 【脊髄萎縮】*myelatrophy *amyelotrophy 【脊髄炎】*myelitis 【脊髄灰白質炎】*poliomyelitis ( 脊髄性小児麻痺、灰白髄炎) 【脊髄空洞症】*syringomyelia 【脊髄出血】*spinal hemorrhage *spinal apoplexy *hematomyelia[] hemorrhagic telangiectasia Hereditary persistence of fetal hemoglobin - beta-thalassemia Hereditary persistence of fetal hemoglobin - sickle cell disease Hereditary thrombophilia[]

  • Cerebrovascular Disorder

    Cerebrovascular disorders are generally rare in children, but among them are: Aneurysms Arteriovenous malformations (AVMs) Moyamoya disease Vein of Galen malformations More[] […] hemorrhage: between the arachnoid and brain or spinal cord Intraparenchymal (intracerebral) hemorrhage: in the brain itself (or less commonly hemorrhage into the spinal cord (hematomyelia[] A Hereditary Hemorrhagic Telangiectasia Center of Excellence, as designated by the HHT Foundation International, Inc.[]

  • Tricho-Retino-Dento-Digital Syndrome

    Ala-D Porphyria, congenital erythropoietic Porphyria, hereditary coproporphyria Portal hypertension due to infrahepatic block Portal hypertension Portal thrombosis Portal vein[] […] polycythemia ( 赤血球増加症) (脊) 【脊髄萎縮】*myelatrophy *amyelotrophy 【脊髄炎】*myelitis 【脊髄灰白質炎】*poliomyelitis ( 脊髄性小児麻痺、灰白髄炎) 【脊髄空洞症】*syringomyelia 【脊髄出血】*spinal hemorrhage *spinal apoplexy *hematomyelia[] […] ataxia variant V1 Telangiectasia, hereditary hemorrhagic Telangiectasia Telecanthus hypertelorism pes cavus Telecanthus with associated abnormalities Telencephalic leukoencephalopathy[]

  • Cobb Syndrome

    AVMs and fistulas are not part of this disorder, for which no genetic cause is known (in contrast with Parkes-Weber and CM-AVM Syndrome).[] Case studies of children younger than 2 years showed that they presented with a significantly lower incidence of hemorrhage, either hematomyelia or subarachnoid hemorrhage[] KTS (Online Mendelian Inheritance in Man, 149000; ) is a relatively uncommon sporadic disorder that primarily consists of the following: 1) a slow-flow vascular malformation[]

  • Spastic Ataxia with Congenital Miosis

    The fundus may have dilated congested veins with some haemorrhages and macular oedema. Management is directed at the cardiovascular disorder.[] Spinal  1. intramedullary:- Syringomyelia, hematomyelia, ependymoma, glioma, astrocytoma  2.Extramedullary :-  2a:-intradural:- meningioma, neurofibroma, arachnoiditis[] Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome) Autosomal Dominant Disorders Autosomal Dominant. Telangiectasias of skin and mucous membranes.[]

  • Hypertrichotic Osteochondrodysplasia

    Genotype-Phenotype Correlations Current information about genotype - phenotype correlation in Cantú syndrome and related disorders is limited.[] […] polycythemia ( 赤血球増加症) (脊) 【脊髄萎縮】*myelatrophy *amyelotrophy 【脊髄炎】*myelitis 【脊髄灰白質炎】*poliomyelitis ( 脊髄性小児麻痺、灰白髄炎) 【脊髄空洞症】*syringomyelia 【脊髄出血】*spinal hemorrhage *spinal apoplexy *hematomyelia[] hereditary hematuria syndrome , see Alport syndrome hereditary hemochromatosis hereditary hemorrhagic telangiectasia hereditary hemorrhagic thrombasthenia , see Glanzmann[]

  • Diffuse Serous Labyrinthitis

    […] obstruction) reported in severe manubriosternal joint disorders (1, 11) .[] Intra-spinal hemorrhage Epidural hematoma (EDH) Subdural hematoma (SDH) SAH subarachnoid hemorrhage (SAH) Cord hematoma (hematomyelia) 8.[] Causes Idiopathic (cause unknown) Hypertension Vascular abnormalities (hereditary hemorrhagic telangiectasia) Trauma: deviation or perforation of the septum Infection (for[]

  • Foix-Alajouanine Syndrome

    Foix-Alajouanine myelitis - a disorder of the lower spinal cord in adult males resulting in progressive paraplegia.[] Applicable To Edema of spinal cord Hematomyelia Nonpyogenic intraspinal phlebitis and thrombophlebitis Subacute necrotic myelopathy The following code(s) above G95.19 contain[] hemorrhagic telangiectasia KTS Klippel-Trenaunay syndrome LM lymphatic malformation M male NA not available/not applicable VEGF vascular endothelial growth factor VM venous[]

  • Shy-Drager Syndrome

    Asthma, Aspirin-Induced Erythrokeratodermia Variabilis Cryopyrin-Associated Periodic Syndromes Peritoneal Fibrosis Carney Complex Leukoencephalopathies Upper Extremity Deep Vein[] […] hypotension may develop in the course of a number of different neurologic diseases. 1-3 Among others, we have encountered it in multiple sclerosis and in a high cervical calcified hematomyelia[] , Hereditary Hemorrhagic Thalamic Diseases Tracheobronchomegaly Tuberous Sclerosis Uveoparotid Fever Spinal Muscular Atrophies of Childhood Wernicke Encephalopathy Dry Eye[]

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