Results 71 to 80 of about 30,124 (290)
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT We report the first female case of Goltz–Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. This case expands the known phenotypic and genotypic spectrum of FDH.
Anna Bolzon +5 more
wiley +1 more source
Acquired port-wine stain in an adult male: First reported case from India with review of literature
Indian Journal of Dermatology, 2015 Port-wine stains (PWSs) are congenital vascular lesions caused by progressive ectasia of blood vessels located in the vascular plexus of the dermis. Acquired PWSs develop later in life but are identical in morphology and histology to the congenital PWSs.
Shuchi Bansal +3 more
doaj +1 more source
Beyond Treatment: The Strategy of Nonintervention in Choroidal Hemangioma
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT The circumscribed choroidal hemangioma (CCH) is a benign congenital eye tumor whose etiology is not clear. A 41‐year‐old female patient came with a 2‐year history of slowly progressive deteriorating vision in her right eye. In the left eye, the best‐corrected visual acuity (BCVA) was 6/6, and counting fingers at 1 m in the right eye.
Humdan Khan +8 more
wiley +1 more source
Sturge Weber Syndrome: A Case Study [PDF]
Journal of Clinical and Diagnostic Research, 2017 The aim of this case review was to touch upon the various clinical presentations and diagnostic features of Sturge-Weber syndrome (SWS) as seen in the dental/medical practice.
Mahesh Neerupakam +3 more
doaj +1 more source
Multifocal Kaposiform Hemangioendothelioma Successfully Treated With Sirolimus Monotherapy
Pediatric Dermatology, Volume 43, Issue 1, Page 158-162, January/February 2026.ABSTRACT Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor that typically presents in infancy and may be associated with the Kasabach–Merritt phenomenon (KMP). We present a challenging case of multifocal KHE on the leg of an infant, initially suspected at birth to be a reticulate port wine birthmark.
Matthew J. Mahoney +8 more
wiley +1 more source
Indian Journal of Ophthalmology, 2017 A 6-year-old girl presented with blurred vision and was found to have elevated intraocular pressure (IOP) and glaucomatous optic disc damage in both eyes.
Manju R Pillai +3 more
doaj +1 more source
Barnes Hospital Bulletin [PDF]
, 1983 https://digitalcommons.wustl.edu/bjc_barnes_bulletin/1213/thumbnail ...
core +1 more source
Advanced Materials, Volume 37, Issue 49, December 10, 2025.This article summarizes significant technological advancements in materials, photonic devices, and bio‐interfaced systems, which demonstrate successful applications for impacting human healthcare via improved therapies, advanced diagnostics, and on‐skin health monitoring.
Seunghyeb Ban +5 more
wiley +1 more source
Pregnancy tumor and facial port-wine stain: A case report
Journal of Craniomaxillofacial Research, 2018 Pyogenic granuloma is a common tumor-like growth of the oral cavity that traditionally has been considered to be non-neoplastic in nature. The pyogenic granuloma is a smooth or lobulated mass that is usually pedunculated, although some lesions are ...
Mohsen Barzegar +5 more
doaj
A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge–Weber Syndrome
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT This rare coexistence of Sturge–Weber Syndrome (SWS) and discoid lupus erythematosus (DLE) presents unique diagnostic and therapeutic challenges. It highlights potential shared environmental triggers and overlapping inflammatory mechanisms, underscoring the need for a multidisciplinary approach to management.
Amir Efazati +4 more
wiley +1 more source