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852 Possible Causes for Ataxia Telangiectasia, Hereditary Hemorrhagic Telangiectasia

  • Generalized Essential Telangiectasia

    Synonym: angioma serpiginosum. (05 Mar 2000) ataxia telangiectasia syndrome ataxia telangiectasia ataxia-telangiectasia An intriguing autosomal recessive disorder in which[kmle.co.kr] Recurrent hemorrhage in the setting of telangiectases, including GI bleeding, is more typically associated with hereditary hemorrhagic telangiectasia.[ncbi.nlm.nih.gov] Date Added: 2018-03-06 Angiokeratoma Angiokeratoma Corporis Diffusum Generalized Essential Telangiectasia Hereditary Hemorrhagic Telangiectasia Mastocytosis Telangiectasia[gulfdoctor.net]

  • Juvenile Polyposis Syndrome

    telangiectasia, and neurofibromatosis.[childrenscolorado.org] Eighty-one percent of SMAD4 patients had hereditary hemorrhagic telangiectasia and 14% were suspected of having hereditary hemorrhagic telangiectasia.[ncbi.nlm.nih.gov] Ataxia with Vitamin E Deficiency Markus Schuelke. Initial Posting: May 20, 2005; Last Update: October 13, 2016. Ataxia-Telangiectasia Richard Gatti and Susan Perlman.[ncbi.nlm.nih.gov]

  • Systemic Scleroderma

    telangiectasia, British Journal of Cancer, 10.1038/sj.bjc.6602658, 93, 2, (260-265), (2005).[doi.org] Multiple telangiectasia, Raynaud’s phenomenon, sclerodactyly, and subcutanious calcinosis: a syndrome mimicking hereditary hemorrhagic telangiectasia.[degruyter.com] L Hammarström, T E Robsahm, H Kääriäinen, A Bregård, K Brøndum-Nielsen, J Yuen and M Tucker, Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia[doi.org]

  • Juvenile Polyp

    telangiectasia, and neurofibromatosis.[childrenscolorado.org] Mutations in the SMAD4 gene are also associated with a juvenile polyposis syndrome-hereditary hemorrhagic telangiectasia (JPS-HHT) phenotype.[genedx.com] Ataxia with Vitamin E Deficiency Markus Schuelke. Initial Posting: May 20, 2005; Last Update: October 13, 2016. Ataxia-Telangiectasia Richard Gatti and Susan Perlman.[ncbi.nlm.nih.gov]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Fewer people than this are carriers of the mutated gene that causes ataxia-telangiectasia.[nhs.uk] Hereditary episodic ataxia Hereditary essential tremor Hereditary hemorrhagic telangiectasia Hereditary leiomyomatosis and renal cell cancer Hereditary motor and sensory neuropathy[sanfordresearch.org] Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome) Autosomal Dominant Disorders Autosomal Dominant. Telangiectasias of skin and mucous membranes.[kumc.edu]

  • Hepatic Arteriovenous Malformation

    Ataxia telangiectasia Ataxia-telangiectasia is an autosomal recessive, multisystem disorder characterized by progressive neurologic impairment, variable immunodeficiency with[ghrnet.org] Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by multisystemic vascular dysplasia.[ncbi.nlm.nih.gov] Abstract Symptomatic hepatic involvement is a rare complication of hereditary hemorrhagic telangiectasia and most commonly consists of fibrosis or cirrhosis.[ncbi.nlm.nih.gov]

  • Sturge-Weber Syndrome

    Pictures Face Legs v t e Phakomatoses and other congenital malformations not elsewhere classified ( Q85-Q89, 759 ) Phakomatoses Abdallat Davis Farrage syndrome - Ataxia telangiectasia[wikidoc.org] Inheritance in Man (OMIM) TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER; HHT -187300 Online Mendelian Inheritance in Man (OMIM) STURGE-WEBER SYNDROME[en.wikipedia.org] Online Mendelian Inheritance in Man (OMIM) PARKES WEBER SYNDROME -608355 Online Mendelian Inheritance in Man (OMIM) TELANGIECTASIA, HEREDITARY BENIGN -187260 Online Mendelian[en.wikipedia.org]

  • Hypogammaglobulinemia

    Hypogammaglobulinemia Drug Induced Antimalarial agents Captopril Carbamazepine Glucocorticoids Fenclofenac Gold salts Penicillamine Phenytoin Sulfasalazine Genetic Disorders Ataxia[esid.org] 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] They include: ataxia-telangiectasia (A-T) autosomal recessive agammaglobulinemia (ARA) common variable immunodeficiency (CVID) hyper-IgM syndromes IgG subclass deficiency[healthline.com]

  • Hereditary Hemorrhagic Telangiectasia

    On DermNet NZ Differential diagnosis of vascular lesions Telangiectasia Ataxia-telangiectasia Generalised essential telangiectasia Other websites The Hereditary Hemorrhagic[dermnetnz.org] Symptomatic Children with Hereditary Hemorrhagic Telangiectasia.[ncbi.nlm.nih.gov] , Type 1 Orw Disease Osler-Rendu-Weber Disease TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER,[wikidata.org]

  • Arteriovenous Malformation

    telangiectasia .[medicinenet.com] Hereditary hemorrhagic telangiectasia (HHT) The natural history of HHT is not well understood.[clinicaladvisor.com] telangiectasia.[medicinenet.com]

Further symptoms

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