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33 Possible Causes for Microcytic Anemia, Plummer-Vinson Syndrome, Shy Drager Syndrome

  • Iron Deficiency Anemia

    The most used name is Plummer-Vinson syndrome, named after Henry Stanley Plummer (1874–1936) and Porter Paisley Vinson (1890–1959) who were physicians on the staff of the[dx.doi.org] Abstract Iron-refractory iron deficiency anemia (IRIDA) is a rare autosomal recessive disease characterized by congenital hypochromic microcytic anemia, low transferrin saturation[ncbi.nlm.nih.gov] Patients have hypochromic microcytic anemia refractory to oral iron and are only partially responsive to parenteral iron administration.[ncbi.nlm.nih.gov]

  • Plummer-Vinson Syndrome

    The authors report the case of a 6 year old with Plummer-Vinson syndrome.[ncbi.nlm.nih.gov] Shy-Drager syndrome シャイ・ドレーガー症候群 GeorgeMilton Shy (1919-1967) American neurologist and Glenn Albert Drager(1917-1967) American physician Sia シア Sia test シア試験;シアテスト Silverman[jams.med.or.jp] Blood tests demonstrate a hypochromic microcytic anemia that is consistent with an iron-deficiency anemia.[en.wikipedia.org]

  • Anemia of Chronic Disease

    Rare symptoms & signs: -Glossitis or angular cheilitis -Dysphagia due to esophageal web (Plummer-Vinson syndrome) -Koilonychia; "Spoon" fingernails -Pica -soreness of mouth[quizlet.com] Conclusions: CD should be included in the differential diagnosis of microcytic anemia.[doi.org] Iron deficiency anemia (IDA) and anemia of chronic disease (ACD) are the most prevalent, both characterized by hypochromic microcytic anemia and low serum iron (SI).[ncbi.nlm.nih.gov]

  • Hallervorden-Spatz Syndrome

    プラマー・ヴィンソン Plummer-Vinson syndrome プラマー・ヴィンソン症候群 HenryStanley Plummer (1874-1937) American internist and endocrinologist and PorterPaisley Vinson (1890-1959.)[jams.med.or.jp] Drager syndrome Shy-Drager syndrome Sporadic olivopontocerebellar atrophy Striatonigral degeneration Clinical Information A progressive neurological disorder characterized[icd9data.com] Here, we report a case of aceruloplasminemia in a teenage girl with hypochromic microcytic anemia.[journals.lww.com]

  • Ayerza Syndrome

    Pickardt Plummer's disease – Henry Stanley Plummer PlummerVinson syndrome (aka Kelly–Patterson syndrome, Paterson–Brown–Kelly syndrome, and Waldenstrom–Kjellberg syndrome[infogalactic.com] Shy-Drager syndrome シャイ・ドレーガー症候群 GeorgeMilton Shy (1919-1967) American neurologist and Glenn Albert Drager(1917-1967) American physician Sia シア Sia test シア試験;シアテスト Silverman[jams.med.or.jp] , Dyserythropoietic, Congenital, see congenital dyserythropoietic anemia Anemia, hereditary sideroblastic, see X-linked sideroblastic anemia anemia, hypochromic microcytic[mygenomics.com]

  • Gaisbock's Syndrome

    Plummer vinson syndrome/Paterson brown kelly syndrome -Combination of symptomatic hypo pharyngeal webs and iron deficiency anemia in mddle aged female.Radiological finding-web[masterofmedicine.com] syndrome シャイ・ドレーガー症候群 GeorgeMilton Shy (1919-1967) American neurologist and Glenn Albert Drager(1917-1967) American physician Sia シア Sia test シア試験 Silverman シルバーマン Silverman[jams.med.or.jp] […] or hypochromic, microcytic anemia Megaloblastic Anemia A group of dso in which the blood and BM hematopoietic cells display changes Pathogenesis: impaired DNA synthesis ([slideserve.com]

  • Unverricht-Lundborg Syndrome

    プラマー・ヴィンソン Plummer-Vinson syndrome プラマー・ヴィンソン症候群 HenryStanley Plummer (1874-1937) American internist and endocrinologist and PorterPaisley Vinson (1890-1959.)[jams.med.or.jp] anemia with liver iron overload Microdeletion 22q11.2 Microdeletion 9q22.3 Microdontia-type I microtia-deafness syndrome Microduplication 17p12 Microduplication Xp11.22p11.23[orpha.net] syndrome シャイ・ドレーガー症候群 GeorgeMilton Shy (1919-1967) American neurologist and Glenn Albert Drager(1917-1967) American physician Sia シア Sia test シア試験 Silverman シルバーマン Silverman[jams.med.or.jp]

  • Salti-Salem Syndrome

    Stalk Interruption Syndrome Piussan Lenaerts Mathieu syndrome Plica syndrome Plummer-Vinson Syndrome Podder-Tolmie Syndrome POEMS syndrome Pointer Syndrome Poland syndrome[rgd.mcw.edu] [ edit ] Shprintzen–Golberg craniosynostosis Shprintzen syndrome Shwachman syndrome Shwachman–Bodian–Diamond syndrome Shwartzman phenomenon ShyDrager syndrome Si [ edit[en.wikipedia.org] anemia with iron overload Hypocomplementemic urticarial vasculitis Hypodermitis sclerodermaformis - See Lipodermatosclerosis Hypodermyasis Hypodontia - dysplasia of nails[herenciageneticayenfermedad.blogspot.com]

  • Nakajo Syndrome

    Stalk Interruption Syndrome Piussan Lenaerts Mathieu syndrome Plica syndrome Plummer-Vinson Syndrome Podder-Tolmie Syndrome POEMS syndrome Pointer Syndrome Poland syndrome[rgd.mcw.edu] Drager Syndrome) MURCS Association ((MU)llerian, (R)enal, (C)ervicothoracic (S)omite abnormalities) Muscular Dystrophy Myasthenia Gravis Myasthenia Gravis Myofibrillar Myopathy[geneticalliance.org.au] This disorder encompasses Nakajo-Nishimura syndrome (NKJO); joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy (JMP syndrome);[diseaseinfosearch.org]

  • Singleton Merten Syndrome

    Stalk Interruption Syndrome Piussan Lenaerts Mathieu syndrome Plica syndrome Plummer-Vinson Syndrome Podder-Tolmie Syndrome POEMS syndrome Pointer Syndrome Poland syndrome[rgd.mcw.edu] Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD) SHORT Syndrome Shwachman Syndrome Shy Drager Syndrome Sialadenitis Sialidosis Sickle Cell Disease Simpson Dysmorphia[medschool.umaryland.edu] […] lipodystrophy, and dermatosis syndrome, Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome, Joint contractures, muscular atrophy, microcytic[genda.com.ar]

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