Results 21 to 30 of about 16,789 (188)
Hemangiomas of the maxillofacial area: Case Report, Classification and Treatment Planning
Open Medicine, 2015 Vascular lesions of the maxillofacial area are even more challenging than in other different body district, because of the high aesthetic and functional relevance of this area for the sense organs presence like eye, brain, tongue, ear and nose. For these
Cortese Antonio +4 more
doaj +1 more source
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Arthrogryposis multiplex congenita (AMC) is defined as the presence of joint contractures affecting at least two body regions at birth. Three different ERGIC1 variants have been reported in individuals with AMC. Here, we report on a 16‐year‐old male with a homozygous ERGIC1 c.250+1G>A variant that was classified as a variant of uncertain ...
Lauren Kerr +7 more
wiley +1 more source
Maffucci's syndrome: A rare case report with unusual location
Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2019 Maffucci's syndrome is a rare nonhereditary syndrome characterized by multiple enchondromas and hemangiomas, which is commonly observed over hands and feet.
Shilpa Laxman Patwekar +3 more
doaj +1 more source
Actas Dermo-Sifiliográficas, 2023 Resumen: El diagnóstico diferencial clínico entre los hemangiomas congénitos (HC) y los infantiles (HI) es complicado pero esencial para el tratamiento.
F.J. Melgosa Ramos +5 more
doaj +1 more source
International Forum of Allergy &Rhinology, EarlyView.ABSTRACT Background The modified endoscopic Denker's (MED) approach provides access to all maxillary sinus (MS) walls for resection of various MS and retromaxillary pathologies, but the anteromedial maxilla has historically been resected. This study determined complication rates and outcomes following MED with pyriform aperture (PA) preservation ...
Yasser Almansour +5 more
wiley +1 more source
Epilepsia, EarlyView.Abstract Epilepsy affects more than 50 million individuals globally and has a substantial genetic component that remains to be completely understood. Traditional studies have focused on severe, early onset cases enrolled through clinical or research settings.
Jessica Castrillon Lal +5 more
wiley +1 more source
Journal of Indian Association of Pediatric Surgeons, 2016 Complete midline sternal cleft is a rare congenital anomaly resulting from failed midline ventral fusion of the sternal bars. Very few cases of complete sternal cleft have been described in literature.
Paras Kothari +5 more
doaj +1 more source
PHACE syndrome with parotid hemangiomas: a unique case report
The Egyptian Journal of Radiology and Nuclear Medicine, 2021 Background PHACE syndrome is a congenital disorder in infants characterized by the presence of large hemangiomas in the cervicofacial region along with congenital anomalies of the cardiovascular system, brain, and eyes.
Muhammad Umer Mukhtar +4 more
doaj +1 more source
Przegląd Dermatologiczny, 2022 Infantile hemangiomas are the most common vascular tumors of infancy. They usually appear within the first few weeks after birth and undergo regression over time, usually by the age of four.
Marta Kurzeja +4 more
doaj +1 more source
Novel planning pipeline utilizing the Surgical Theater system for pediatric epilepsy surgery
Epilepsia Open, EarlyView.Abstract Objective Advances in the analysis and collation of radiographic datasets have enhanced presurgical planning for various neurosurgical procedures, including clipping of cerebral aneurysms, surgical resection of tumors, and arteriovenous malformation management.
Lisa B. E. Shields +4 more
wiley +1 more source