Results 131 to 140 of about 7,512,016 (281)

Chronic granulomatous disease: Case series

Pediatric Hematology Oncology Journal, 2016
Purva Kanvinde, Prasad Taur, Ankit Parmar, Naseer, Mukesh Desai, Manisha Madkaikar, Manasi Kulkarni, Mrinal Joshirao, Sangita Mudaliyar, Archana Swami, Nitin Shah, Bharat Agrawal   +11 more
doaj   +1 more source

Chronic granulomatous disease and neovascularisation causing a vitreous haemorrhage.

, 2010
The authors report the case of a 9-year-old boy with chronic granulomatous disease with longstanding inactive chorioretinal lesions developing a spontaneous vitreous haemorrhage.
Baxter, Julia, Gandhewar, Ravikiran, Holden, Roger   +2 more
core   +1 more source

Fibrillar‐Type Dermatitis Herpetiformis: An Underrecognized Variant That Is Rarely Associated With Celiac Disease and Lacking Epidermal Transglutaminase Deposition: A Report of Two Cases

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Dermatitis herpetiformis (DH) is a rare, intensely pruritic cutaneous manifestation of celiac disease (CD), typically presenting with excoriated papulovesicular lesions on extensor surfaces. DH is associated with IgA autoantibodies against epidermal transglutaminase (eTG), which form granular immune deposits in the papillary dermis and induce ...
Jeffrey Damman, Elodie Mendels, Sven van der Woude, Sharon Veenbergen, Gilles F. H. Diercks, Martijn B. van Doorn   +5 more
wiley   +1 more source

Unmasking Iododerma: A Distinctive Histopathologic Pattern of Neutrophil‐Rich Dermatosis With Haloed Cryptococcoid Bodies in the Setting of Hydralazine Exposure and Autoimmune Serologic Abnormalities

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Cutaneous iododerma is a rare adverse reaction to iodine‐containing compounds that may clinically and histopathologically mimic infection, vasculitis, malignancy, and other neutrophilic dermatoses. Although most commonly associated with iodinated contrast exposure, a variety of predisposing factors and potential associations have been reported,
Volha Lenskaya, Ana M. Ciurea, Mika Tabata, Teny M. John, Woo Cheal Cho   +4 more
wiley   +1 more source

Chronic granulomatous disease

, 2019
Chronic granulomatous disease (CGD) is defined as an inherited phagocyte disorder causing defective superoxide generation and intracellular killing.
Siti Nor Hidayah Binti Kamarulzaman
core  

Inborn errors of immunity in children with neuroinflammation

Developmental Medicine &Child Neurology, EarlyView.
Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu, Dilan Dissanayake, Jessie Cunningham, Helen Branson, Ori Scott, E Ann Yeh   +5 more
wiley   +1 more source

Escleromalacia necrotizante: a propósito de 1 caso Scleritis necroticans: Apropos of a case

Revista Cubana de Oftalmología, 2003
La escleromalacia necrotizante es una enfermedad granulomatosa crónica de la esclera, poco frecuente. Se presenta el caso de una paciente femenina, blanca de 63 años de edad con esta afección y se resaltan tanto las manifestaciones oftalmológicas como ...
Ileana Agramonte Centelles, Marta Herrera Soto, Clara Gómez Cabrera, Nereyda Martínez Suárez   +3 more
doaj  

Chronic Granulomatous Disease in an Adult [PDF]

Journal of the Royal Society of Medicine, 1979
D A, Burns, I, Sarkany
openaire   +2 more sources

Tactile Perception of 3D‐Printed Typodont Materials in Dental Education: A Systematic Review

European Journal of Dental Education, EarlyView.
ABSTRACT Background Adoption of additive manufacture of printed typodonts within dentistry for education occurs despite inadequate reproduction of desirable tactile characteristics of human tooth tissues. Variable findings regarding material properties and educational outcomes of 3D‐printed typodonts are reported.
Alice M. G. Cheadle, Reece Bushell, William M. Palin, Phillip L. Tomson, Zehra Yonel, Mohammed A. Hadis   +5 more
wiley   +1 more source

Comparative diagnostic challenges in two horses with skin fragility disorders

Equine Veterinary Education, EarlyView.
Summary Hereditary equine regional dermal asthenia (HERDA) is an autosomal recessive connective tissue disorder of horses caused by a missense mutation (c.115G>A) in the peptidyl‐prolyl cis–trans isomerase B (PPIB) gene, resulting in defective collagen organisation.
M. Biolchi, F. A. Saiki, T. G. Cristo, M. C. Silva, R. J. Souza, A. F. Souza, R. A. Casagrande, J. H. Fonteque, C. I. G. Vogel   +8 more
wiley   +1 more source