Results 141 to 150 of about 214,676 (297)
Journal of Anatomy, Volume 248, Issue 1, Page 40-52, January 2026.This quantitative study identified distinct cranial vault morphologies in Apert and Crouzon syndromes, with a larger anterior fossa in Apert and high variability in Crouzon, reflecting different patterns of suture closure. Abstract Craniosynostoses are congenital conditions characterized by premature suture fusions, altering skull growth and ...
Ombline Delassus +9 more
wiley +1 more source
Prompt versus delayed amniotic membrane application in a patient with acute Stevens-Johnson syndrome
Clinical Ophthalmology, 2013 Jessica B Ciralsky, Kimberly C SippelDepartment of Ophthalmology, Weill Cornell Medical College, New York, NY, USABackground: Stevens-Johnson syndrome is often associated with blinding ocular surface cicatricial sequelae.
Ciralsky JB, Sippel KC
doaj
Medicinal Plants for Acne Vulgaris: An Evidence‐Based Review of Treatments Promoted by Social Media
Journal of Cosmetic Dermatology, Volume 25, Issue 1, January 2026.ABSTRACT Background Acne vulgaris refers to a chronic inflammatory state of the pilosebaceous follicles that affects the majority of adolescents. Treatments encompass topical agents and systemic therapies. Nowadays, we encounter a growing tendency to use herbal remedies, which raises concerns about misinformation disseminated by digital platforms.
Mohammad Mahdi Parvizi +6 more
wiley +1 more source
Drug‐Induced Fuchs Syndrome With Isolated Oral Involvement: A Rare Case Report
Case Reports in Dermatological Medicine, Volume 2026, Issue 1, 2026.Stevens–Johnson syndrome (SJS) is a rare, potentially life‐threatening mucocutaneous disorder characterized by epidermal necrosis and mucosal bullous lesions involving less than 10% of the total body surface area. The majority of cases are aggravated by delayed hypersensitivity reactions to medications.
Salina Paudel +6 more
wiley +1 more source
Pyoderma Gangrenosum as the First Manifestation of Inflammatory Bowel Disease: A Case Report
Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.Approximately 50% of patients with inflammatory bowel disease (IBD) exhibit extraintestinal manifestations, among which skin and mucosal lesions are common. However, pyoderma gangrenosum occurs in only 1%‐2% of IBD patients. We report the case of a 23‐year‐old male patient who was admitted to the hospital with pyoderma gangrenosum that was unresponsive
Nam Hoai Nguyen +7 more
wiley +1 more source
Conjunctival squamous metaplasia on amniotic membrane in Stevens-Johnson syndrome: a case report
BMC OphthalmologyBackground To present a case of conjunctival growth on the amniotic membrane and subsequent pathology revealing conjunctival squamous metaplasia in a patient with Stevens-Johnson syndrome.
Yung-Kang Chen +3 more
doaj +1 more source
Oxcarbazepine-induced Stevens–Johnson syndrome: a pediatric case report [PDF]
, 2017 Burçin Beken +4 more
openalex +1 more source
Scientifica, Volume 2026, Issue 1, 2026.Epilepsy is a neurological disorder characterized by repeated, unprovoked seizures arising from abnormal electrical activity in the brain. The management of epilepsy presents several significant challenges. One of these challenges involves drug resistance, where seizures persist despite treatment with multiple antiepileptic drugs, requiring a tailored ...
Mukul Shyam +5 more
wiley +1 more source
Levofloxacin and Ibuprofen Leading to Steven Johnson Syndrome: A Dermatological Emergency
Journal of Rawalpindi Medical College, 2018 Stevens-Johnson syndrome is a rare, serious disorder of your skin and mucous membranes. It's usually a reaction to a medication or an infection. Often, it begins with flu-like symptoms, followed by a painful red or purplish rash that spreads and blisters.
Muhammad Raheel Zafar et al.,
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Stevens — Johnson syndrome [PDF]
Russian Medical Review, 2020 G.M. Nurtdinova +3 more
openaire +1 more source