0000000000057367

AUTHOR

Maria Concetta Muscia

showing 3 related works from this author

The care pathway for children with urticaria, angioedema, mastocytosis

2015

Cutaneous involvement characterized by urticarial lesions with or without angioedema and itch is commonly observed in routine medical practice. The clinical approach may still remain complex in real life, because several diseases may display similar cutaneous manifestations. Urticaria is a common disease, characterized by the sudden appearance of wheals, with/without angioedema. The term Chronic Urticaria (CU) encompasses a group of conditions with different underlying causes and different mechanisms, but sharing the clinical picture of recurring wheals and/or angioedema for at least 6 weeks. Hereditary Angioedema (HAE) is a rare disorder characterized by recurrent episodes of non-pruritic,…

lcsh:Immunologic diseases. AllergyPulmonary and Respiratory MedicineAllergyUrticariaEpidemiologyImmunologyReviewClinical practiceAngioedema; Children; Clinical practice; Diagnosis; Epidemiology; Itch; Management; Mastocytosis; Skin; UrticariaItchC1-inhibitor030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineimmune system diseasesEdemaDiagnosismedicineImmunology and AllergyAngioedemaskin and connective tissue diseasesChildrenSkinbiologyAngioedemabusiness.industryAutosomal dominant traitAngioneurotic oedemamedicine.diseasePathophysiologyManagement3. Good healthUrticaria Angioedema Mastocytosis Skin Itch Children Epidemiology Diagnosis Management Clinical practice.030228 respiratory systemImmunologyHereditary angioedemabiology.proteinmedicine.symptomlcsh:RC581-607businessMastocytosisWorld Allergy Organization Journal
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Ipertransaminasemia: analisi di una casistica di bambini ricoverati presso la UO "Clinica Pediatrica" Ospedale dei Bambini "G. Di Cristina" di Palerm…

2015

Settore MED/38 - Pediatria Generale E SpecialisticaAST-ALT NAFLD
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Non c'é due senza tre: una sindrome autoinfiammatoria "complessa"

2014

Settore MED/38 - Pediatria Generale E SpecialisticaSindrome autoinfiammatoria Sclerosi multipla gene MEFV gene SM
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