Results 61 to 70 of about 5,302 (181)
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Williams syndrome (WS) is a rare congenital multi‐systemic condition due to gene deletion. We present a rare case of co‐existence of WS, port wine stains, and phacomatosis pigmentovascularis. This case emphasizes the importance of recognizing the co‐occurrence of such conditions and WS for accurate diagnosis and management.
Bahareh Abtahi‐Naeini +2 more
wiley +1 more source
G Protein‐Coupled Receptor Signaling: Implications and Therapeutic Development Advances in Cancers
MedComm, Volume 6, Issue 10, October 2025.G protein‐coupled receptors (GPCRs) are the dynamic protein family in the human genome. GPCR dysregulation aids in the advancement of cancer through increased migration, survival, and proliferation. Novel treatments that target GPCR signaling include orthosteric ligands, biased receptor mutants, PROTACs, and antibody–drug conjugates.
Inamu Rashid Khan +6 more
wiley +1 more source
Epilepsia, Volume 66, Issue 10, Page 3730-3740, October 2025.Open‐label CBD treatment was associated with sustained seizure reduction through 144 weeks, with a consistent safety profile in patients with treatment‐resistant focal epilepsies, regardless of epilepsy type. Abstract Objective Cannabidiol (CBD) treatment was associated with long‐term seizure reduction in patients with various treatment‐resistant ...
Anup D. Patel +8 more
wiley +1 more source
The Phakomatosis (Neurocutaneous Syndromes): Sturge-Weber Syndrome
مجله دانشکده پزشکی اصفهان, 2008 Neurocutaneous syndromes or phakomatosis are inherited or sporadic conditions that feature lesions of both skin and nervous system. Sturge-weber syndrome (SWS) is characterized by a facial cutaneaous angioma (port-wine nevus) and an associated ...
Ahmad Chitsaz
doaj
Targeted Medical Therapies for Vascular Anomalies: A Clinical Review
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Volume 199, Issue 3, Page 161-175, September 2025.ABSTRACT Vascular anomalies represent a broad spectrum of disorders characterized by aberrant blood or lymphatic vessel development, which can lead to complex clinical phenotypes. Historically, vascular anomalies were classified solely on the basis of their clinical and histopathologic features.
Whitney Eng
wiley +1 more source
Anaesthetic Management of A Patient with Sturge-Weber Syndrome Undergoing Oophorectomy
Indian Journal of Anaesthesia, 2009 The Sturge-Weber Syndrome (SWS) is a neurocutaneous disorder characterized by leptomeningeal and facial angiomas, neurologic and ocular manifestations. We report a case of oophorectomy for ovarian dermoid in a 14 year -old girl who was a diagnosed case ...
Manju Gandhi +3 more
doaj
Spectrum of CT and MR findings in Sturge-Weber syndrome: A case report
Medical Journal of Dr. D.Y. Patil University, 2014 Sturge-Weber syndrome is an uncommon, sporadically occurring neurocutaneous syndrome characterized by port wine stain (facial nevus flammeus), congenital glaucoma, and anomalous leptomeningeal angiomatous malformation.
Pallavi J Agrawal +3 more
doaj +1 more source
Annals of the Child Neurology Society, Volume 3, Issue 4, Page 326-329, December 2025.
Katharine E. Joslyn +4 more
wiley +1 more source
Sturge-Weber Syndrome : A Report Of Three Cases
Indian Journal of Dermatology, 2001 Three cases of Sturge â€" Weber syndrome are being reported. All our cases had incomplete form of Sturge- Weber syndrome. They had cutaneous facial angiomas and leptomeningeal agiomas evidenced by central nervous system manifestations (
Jeevankumar B, Mohan Thappa Devinder
doaj
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2008 A síndrome de Sturge-Weber é doença congênita esporádica composta por malformação capilar dérmica facial na área do ramo oftálmico do nervo trigêmio, associada a malformações vasculares das leptomeninges e dos olhos.
Maria Ester Massara Café +2 more
doaj +1 more source