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368 Possible Causes for Hereditary Hemorrhagic Telangiectasia, Pediatric Disorder, Vein Disorder

  • Hereditary Hemorrhagic Telangiectasia

    The monoclonal antibody bevacizumab, seems to be a good option in this disorder.[ncbi.nlm.nih.gov] HHT is a disorder in which some blood vessels do not develop properly.[cdc.gov] Symptomatic Children with Hereditary Hemorrhagic Telangiectasia.[ncbi.nlm.nih.gov]

  • Arteriovenous Malformation

    National Institute of Neurological Disorders and Stroke. 4 Feb. 2013.[medicinenet.com] Arteriovenous malformation (AVM) is a vascular disorder in which arteries and veins are connected directly rather than through capillaries.[vascularcures.org] Hereditary hemorrhagic telangiectasia (HHT) The natural history of HHT is not well understood.[clinicaladvisor.com]

  • Von Willebrand Disease

    , the most common inherited bleeding disorder.[ncbi.nlm.nih.gov] John Akabutu Comprehensice Centre for Bleeding DisordersPediatric Division Stollery Children’s Hospital Clinic Director Dr.[hemophilia.ca] Warad, Pediatric Coagulation Disorders, Pediatrics in Review, 37, 7, (279), (2016).[doi.org]

  • Arteriovenous Fistula

    disorders[ncbi.nlm.nih.gov] This disorder may appear in a manner suggesting deep vein thrombosis or arterial insufficiency of a lower extremity, but the presence of an abdominal bruit and a lower abdominal[link.springer.com] Often diagnosed in childhood, about 30% are associated with hereditary hemorrhagic telangiectasia.[ncbi.nlm.nih.gov]

  • Hereditary Coagulopathy

    These are usually vein clots, such as deep vein thrombosis, but occasionally this disorder can be associated with arterial clots Prothrombin Gene mutation 020210 : an inherited[pediatricstroke.org] The new third edition of Pediatric Stroke and Cerebrovascular Disorders provides a modern clinical approach to managing stroke and other cerebrovascular problems in infants[books.google.de] Hereditary hemorrhagic telangiectasia. N Engl J Med . 1995 Oct 5. 333(14):918-24. [Medline] . Nanda S, Bhatt SP.[emedicine.medscape.com]

  • Coagulation Abnormalities

    BACKGROUND: Legg-Calvé-Perthes disease is a pediatric disorder characterized by osteonecrosis of the proximal femoral epiphysis.[ncbi.nlm.nih.gov] After evaluation, it turned out that she had a myeloproliferative disorder and portal vein thrombosis secondary to that.[ncbi.nlm.nih.gov] Hereditary hemorrhagic telangiectasia (also called Osler-Weber-Rendu Syndrome) is a hereditary disorder of vascular malformation.[msdmanuals.com]

  • Recurrent Thrombophlebitis due to Hereditary Disorders

    […] worse STP encroaching on the deep vein system Underlying clotting disorders[wivein.com] Pediatric disorders associated with genetic thrombophilia include neonatal purpura fulminans, renal vein thrombosis, vena cava thrombosis and hepatic venous thrombosis.[thrombosisjournal.biomedcentral.com] Keywords Hereditary hemorrhagic telangiectasia; Perioperative care; Venous thrombosis Introduction Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu[omicsonline.org]

  • Winchester Syndrome

    […] misalignment of the pulmonary vessels , see alveolar capillary dysplasia with misalignment of pulmonary veins Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency -[herenciageneticayenfermedad.blogspot.com] Definition / general Rare hereditary pediatric disorder with extracellular hyaline material deposition in skin, soft tissue and bone Terminology Molluscum fibrosum in children[pathologyoutlines.com] hemorrhagic telangiectasia Synonym(s): - Winchester syndrome Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic[csbg.cnb.csic.es]

  • Hypogammaglobulinemia

    Immunoglobulins are given through a vein or by injection to boost the immune system. A bone marrow transplant may be considered.[nlm.nih.gov] Sensorineural hearing loss in primary antibody deficiency disorders. J Pediatr. 2008 Aug. 153(2):293-6. [Medline].[emedicine.com] hemorrhagic telangiectasia ) TGFBR1 / TGFBR2 ( Loeys–Dietz syndrome ) GC GUCY2D ( Leber's congenital amaurosis 1 ) JAK-STAT Type I cytokine receptor : GH ( Laron syndrome[en.wikipedia.org]

  • Cutis Marmorata

    In some cases, doctors may need to examine the individual in question in order to determine there is no underlying disorder present.[humanitas.net] M-CMTC is a multisystem disorder and a team of specialist pediatrics, dermatology, neurology and radiology is needed to diagnose and treat such patients.[ijpd.in] Gardner-Diamond Syndrome Hereditary Benign Telangiectasia hereditary hemorrhagic telangiectasia Hypotrichosis-Lymphedema-Telangiectasia Syndrome Kawasaki disease Livedo Reticularis[rgd.mcw.edu]

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