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506 Possible Causes for 010, FAMILY, HSP

  • Acute Gastroenteritis

    Abstract Anaphylactoid purpura, also known as Henoch-Schönleinpurpura (HSP), is an IgA-mediated vasculitis that tends to be a benign disease of childhood.[] Janeiro, RJ, CEP 20550-200, Brazil 4 4 Setor de Pediatria, Hospital Municipal Salles Neto, Praça Condessa Paulo de Frontin 52, Rio Comprido, Rio de Janeiro, RJ, CEP 20260-010[] Lower income families may, rationally, apply a different threshold for seeking treatment than higher income families.[]

  • Hereditary Spastic Paraplegia

    What is Hereditary Spastic Paraplegia?[] Neurogenetics. 2010 Oct;11(4):441-8. doi: 10.1007/s10048-010-0249-2. Epub 2010 Jul 1.[] DNA sequencing showed that he, along with other family members (n 5; mean LDL cholesterol 0.8 mmol/L, apoB 0.31 g/L), were heterozygous for a single nucleotide deletion in[]

  • Campylobacter Jejuni

    Extensive workup revealed no signs of skin or joint disease, thus excluding Henoch-Schönlein purpura.[] RML Institute of Medical Sciences, Lucknow 226 010, India.[] Abstract We describe an outbreak of Campylobacter jejuni enteritis involving three family members of whom one developed Guillain-Barré syndrome (GBS).[]

  • Factor XII Deficiency

    We have experienced a rare case of FXII deficiency in a patient previously diagnosed with hereditary spastic paraplegia (HSP).[] Clin Exp Nephrol. 2011 Apr;15(2):269-74. doi: 10.1007/s10157-010-0375-z. Epub 2011 Jan 27.[] Abstract The case of a patient with Hageman trait and his family study are reported.[]

  • Leukopenia

    These findings may further support the importance of complement activation in the pathogenesis of HSP.[] Ir J Med Sci. 2012 Mar;181(1):139-41. doi: 10.1007/s11845-010-0587-y. Epub 2010 Sep 26.[] Abstract A young patient with familial Mediterranean fever (FMF) developed leukopenia each time she took colchicine.[]

  • Orchitis

    Abstract Henoch-Schönlein purpura (HSP) is the most common cause of nonthrombocytopenic purpura in children.[] Pediatr Radiol. 2010 Dec;40 Suppl 1:S21-3. doi: 10.1007/s00247-010-1676-9. Epub 2010 May 1. Author information 1 Department of Urology, Mayo Clinic, 5777 E.[] Here, by utilizing a forward genetic approach, we identified kinesin family member 1C (Kif1c) as a positional candidate for Orch3 and, using a transgenic approach, demonstrated[]

  • Leukodystrophy

    One recessive mutation (p.Ile33Met) has been associated with a much milder phenotype--hereditary spastic paraplegia type 44.[] Neurogenetics. 2011 Feb;12(1):73-8. doi: 10.1007/s10048-010-0256-3. Epub 2010 Aug 19.[] Because the patients did not show adducted thumbs or hydrocephalus, the L1CAM change in this family can be interpreted as different scenarios.[]

  • Rett Syndrome

    In addition, a substantial decrease in the expression of nine members of the heat shock protein (HSP) family was found in the 5-week samples, but not at 24 weeks.[] Neurogenetics. 2011 Feb;12(1):1-8. doi: 10.1007/s10048-010-0255-4. Epub 2010 Aug 24.[] Analyses also explored family functioning as a mediator of the relationship between other variables and adaptation.[]

  • Subacute Thyroiditis

    Serologically proven mumps infection was detected and may have been a triggering factor in the development of both HSP and subacute thyroiditis.[] Endocrine. 2010 Jun;37(3):440-1. doi: 10.1007/s12020-010-9327-3. Epub 2010 Mar 30. Author information 1 Internal Medicine Department, General Hospital G.[] Abstract Although subacute thyroiditis (de Quervain's thyroiditis) is presumed to be caused by a viral infection, only 2 familial occurrences of subacute thyroiditis have[]

  • Rapidly Progressive Glomerulonephritis

    Abstract We report here the autopsy findings in a 51-year-old man who had been admitted with Henoch-Schönlein purpura (HSP) accompanied by rapidly progressive glomerulonephritis[] Clin Exp Nephrol. 2010 Dec;14(6):598-601. doi: 10.1007/s10157-010-0312-1. Epub 2010 Jul 14.[] Abstract Two familial clusters of systemic vasculitis are described.[]