Results 41 to 50 of about 10,590 (323)
Glanzmann′s thrombasthenia: A case report and review
Journal of Indian Academy of Oral Medicine and Radiology, 2011 Glanzmann′s thrombasthenia (GT) is a rare autosomal recessive disorder and characterized by a lack of platelet aggregation due to the absence of platelet glycoprotein (GP) Ilb and Illa. Usually, the disease leads to mild hemorrhage but sometimes bleeding
Ajit D Dinkar +2 more
doaj +1 more source
Refractory Severe Thrombocytopenia during Pregnancy: How to Manage [PDF]
Revista Brasileira de Ginecologia e Obstetrícia, 2018 Thrombocytopenia is the most common hemostatic change in pregnancy, but severe thrombocytopenia is rare. One of the causes, immune thrombocytopenic purpura (ITP), is characterized by increased platelet destruction by immunoglobulin G (IgG) antibodies ...
Joana Gomes de Amorim +2 more
doaj +1 more source
American Journal of Hematology, EarlyView.ABSTRACT Non‐severe aplastic anemia (NSAA) is a heterogeneous bone marrow failure syndrome with limited standardized treatment options. Cyclosporine A (CsA) monotherapy often yields suboptimal responses, highlighting an unmet clinical need for more effective therapies.
Lele Zhang +18 more
wiley +1 more source
Multiple autoimmune syndrome complicating the management of diabetic retinopathy
American Journal of Ophthalmology Case Reports, 2020 Purpose: To describe a case of multiple autoimmune syndrome presenting with type I diabetes, choroidal vitiligo, coeliac disease, pseudohypoparathyroidism, and immune thrombocytopenia purpura (ITP), the latter diagnosed seven years after the initial ...
Anmar Abdul-Rahman, FRANZCO, MOphth
doaj +1 more source
External cervical root resorption involving multiple maxillary teeth in a patient with hereditary hemorrhagic telangiectasia [PDF]
, 2005 Hereditary hemorrhagic telangiectasia (HHT) is an inherited syndrome characterized by mucocutaneous telangiectases that commonly involve the tongue, lips, fingers, and conjunctiva.
Edwards, Paul C., McVaney, Tim
core +1 more source
Clinical Advances in Periodontics, EarlyView.ABSTRACT Background To evaluate the efficacy and long‐term clinical outcomes of the one‐stage procedure for covering isolated deep gingival recessions (GRs) in the mandibular anterior region employing a laterally positioned flap (LPF) with a connective tissue graft (CTG), with a retrospective case series.
Lucrezia Parma‐Benfenati +1 more
wiley +1 more source
Periodontitis treatment and microbiome in a patient with FAM20A mutation: Case study of 1.5 years
Clinical Advances in Periodontics, EarlyView.Abstract Background Enamel‐renal‐gingival syndrome (ERGS) is an autosomal recessive disorder caused by mutations in the FAMily with sequence similarity 20A (FAM20A) gene, and is characterized by amelogenesis imperfecta, delayed or failed tooth eruption, and periodontitis.
John Rong Hao Tay +2 more
wiley +1 more source
A novel clinical protocol for the greater palatine compression suture: A case report
Journal of Indian Society of Periodontology, 2018 Bleeding from the palatal donor site is a worrisome complication of palatal soft tissue harvesting procedures and leads to considerable stress to both the patient and the surgeon.
Mihir Raghavendra Kulkarni +3 more
doaj +1 more source
Erythema multiforme-like lip presentation in pemphigus vulgaris patients: a multicenter case series
BMC Oral Health, 2023 Pemphigus vulgaris (PV) is a chronic autoimmune mucocutaneous blistering disease. Autoantibodies are directed against desmogleins, leading to the formation of intraepithelial bullae. PV, as with other autoimmune mucocutaneous disorders of the oral cavity,
Ghidaa Subahi +6 more
doaj +1 more source