- Oni L, Sampath S. Childhood IgA Vasculitis (Henoch Schonlein Purpura)-Advances and Knowledge Gaps. (medscape.com)
- He also had severe complications of gastrointestinal bleeding, extensive leukocytoclastic skin vasculitis, renal, and neurological manifestations. (unair.ac.id)
- Comparison between adults and children with Henoch-Schönlein purpura nephritis. (medscape.com)
- Goldstein AR, White RH, Akuse R, Chantler C. Long-term follow-up of childhood Henoch-Schönlein nephritis. (medscape.com)
- Ronkainen J, Nuutinen M, Koskimies O. The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study. (medscape.com)
- Early onset seen in infants can be accompanied with severe renal insufficiency while in adulthood the renal damage can be less severe. (wikipedia.org)
- Particular attention was paid to congenital syndrome, such as Vacterl, Fabry and Goldenhar syndrome and acquired conditions such as Schoenlein-Henoch disease potentially leading to renal impairment. (biolifesas.org)
- [ 1 ] Acquired FXIII deficiencies, which result from autoantibodies against FXIII subunits, are extremely rare but may produce severe bleeding diatheses. (medscape.com)
- However, these tests cannot be used to screen for FXIII deficiency because the results would be within reference ranges in a patient with isolated severe FXIII deficiency. (medscape.com)
- To date, most identified mutations leading to severe FXIII deficiency and a bleeding disorder involve subunit A, with very few mutations reported involving subunit B. The gene for subunit A is located on chromosome 6 bands p24-25. (medscape.com)
- Albrotran is indicated in the treatment of severe or complicated urinary tract infections in adults and pediatric patients two months of age and older due to susceptible strains of Escherichia coli, Klebsiella species, Enterobacter species, Morganella morganii and Proteus species when oral administration of Albrotran is not feasible and when the organism is not susceptible to single-agent antibacterials effective in the urinary tract. (pillintrip.com)
- Case presentation: A 65-year-old Indonesian male with severe complications of HSP had been reported. (unair.ac.id)
- Putri, AT & Awalia 2022, ' Diagnosis and management of Henoch-Schonlein purpura in Indonesian elderly with severe complication: A rare case ', Annals of Medicine and Surgery , vol. 77, 103650. (unair.ac.id)
- Two patients are described with severe MVS, pulmonary venous hypertension and enlarged mediastinal, pulmonary and hilar lymph nodes. (the-medical-dictionary.com)
- Henoch-Schönlein Purpura in Children: An Updated Review. (medscape.com)
- Henoch Schonlein Purpura in children: clinical analysis of 120 cases. (medscape.com)
- Fifteen-year experience of children with Henoch-Schonlein purpura in southern Taiwan, 1991-2005. (medscape.com)
- Henoch-Schoenlein purpura (HSP) affects approximately 20 in 100,000 children per year and twice as many boys than girls are diagnosed with it usually between 5 and 15 years of age. (prn.org.au)
- Bulun A, Topaloglu R, Duzova A, Saatci I, Besbas N, Bakkaloglu A. Ataxia and peripheral neuropathy: rare manifestations in Henoch-Schönlein purpura. (medscape.com)
- Background: Henoch-Schonlein purpura (HSP) in the elderly is very rare, so this case report was conducted to improve the diagnosis and management of HSP. (unair.ac.id)
- Conclusion: Management of HSP in the elderly patient is challenging as it is a rare case, with a tendency for severe manifestations and rapid progression. (unair.ac.id)
- Peeters V, De Raeve L. Blistering eruptions in Henoch-Schönlein syndrome: more common than assumed. (medscape.com)
- Henoch Schonlein purpura in childhood: epidemiological and clinical analysis of 150 cases over a 5-year period and review of literature. (medscape.com)
- Heterozygous parents of a propositus with severe bleeding usually are asymptomatic, although some cases of bleeding in heterozygotes have been reported. (medscape.com)
- Severe gastrointestinal vasculitis in Henoch-Schoenlein purpura: pathophysiologic mechanisms, the diagnostic value of factor XIII, and therapeutic options. (medscape.com)
- In medicine (rheumatology and pediatrics) Henoch-Schönlein purpura (HSP, also known as allergic purpura ) is a form of vasculitis that mainly affects children. (the-medical-dictionary.com)
- Early onset seen in infants can be accompanied with severe renal insufficiency while in adulthood the renal damage can be less severe. (wikipedia.org)
- A severe, rapidly fatal reaction occurring most commonly in children following an infectious illness. (nih.gov)
- In rare instances, a skin rash may be followed by a more severe reaction, such as Stevens-Johnson syndrome, toxic epidermal necrolysis, hepatic necrosis, and serious blood disorders (see PRECAUTIONS). (nih.gov)
- Severe cases of thrombocytopenia that are fatal or life threatening have been reported. (nih.gov)
- 10. Glomerulocystic disease: a severe form in a monozygous twin. (nih.gov)
- Shanbhag S, Ghosh K, Shetty S. Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations. (medscape.com)
- Lagatrim Forte is indicated in the treatment of severe or complicated urinary tract infections in adults and pediatric patients two months of age and older due to susceptible strains of Escherichia coli, Klebsiella species, Enterobacter species, Morganella morganii and Proteus species when oral administration of Lagatrim Forte is not feasible and when the organism is not susceptible to single-agent antibacterials effective in the urinary tract. (pillintrip.com)