Results 31 to 40 of about 5,117 (135)

Ultrasound findings associated with neonatal acute liver failure secondary to gestational alloimmune liver disease: A case series

JPGN Reports, EarlyView.
Abstract Objectives Gestational alloimmune liver disease is the leading cause of neonatal acute liver failure, hypothesized to emerge from maternal exposure to an antigen that is expressed on fetal hepatocytes, resulting in maternal‐fetal alloimmune attack and activation of the complement cascade.
Naseem Ravanbakhsh, Ashley M. Upton, Chun‐Sing Huang, Nhu Thao N. Galván, John Goss, Sanjiv Harpavat, Jose A. Hernandez   +6 more
wiley   +1 more source

Comparative Assessment of 532/1064‐nm KTP/Nd: YAG and 595‐nm Pulsed Dye Laser for Cutaneous Vascular Lesions: A Prospective Split‐Site Study

Lasers in Surgery and Medicine, EarlyView.
ABSTRACT Objectives This exploratory pilot study aims to characterize effective laser settings and evaluate the clinical outcomes and tolerability of a dual‐wavelength 532/1064‐nm KTP/Nd: YAG laser system compared to a 595‐nm pulsed dye laser with cryogen spray cooling, across multiple vascular indications, including port‐wine capillary malformations ...
Olamide Sonuga Finney, Feben Messele, Karishma S. Shah, Cameron Zachary, Sungat Grewal, Kristen M. Kelly   +5 more
wiley   +1 more source

Blinded by the Bot: Benchmarking GPT and Gemini Against Human Authors in Otolaryngology Reviews

World Journal of Otorhinolaryngology - Head and Neck Surgery, EarlyView.
ABSTRACT Objective To compare the quality of scientific review articles generated by two artificial intelligence systems, ChatGPT and Gemini, with those written by human authors in the field of otolaryngology. Methods Two otolaryngology topics, chronic rhinosinusitis and infantile subglottic hemangioma, were selected.
Sholem Hack, Rebecca Attal, Letizia Nitro, Cecilia Rosso, Anastasia Urbanelli, Antonio Mario Bulfamante, Luigi Angelo Vaira, Omar G. Ahmed, Masayoshi Takashima   +8 more
wiley   +1 more source

Influencing Factors Associated With Infantile Hemangioma: A Case–Control Study Among Chinese Pediatric Populations

The Journal of Dermatology, EarlyView.
ABSTRACT Infantile hemangioma (IH) is the most common benign vascular tumor of infancy. While its epidemiology is well‐documented in Caucasian populations, large‐scale systematic studies regarding clinical characteristics and risk factors in the Chinese population remain limited.
Xinyu Liu, Dan Song, Liang Wang, Changfeng Wang, Lei Guo   +4 more
wiley   +1 more source

Two Cases of Oculofaciocardiodental (OFCD) Syndrome due to X-Linked BCOR Mutations Presenting with Infantile Hemangiomas: Phenotypic Overlap with PHACE Syndrome

Case Reports in Genetics, 2019
Background. Oculofaciocardiodental (OFCD) syndrome is due to mutations in BCOR (BCL-6 corepressor). OFCD has phenotypic overlaps with PHACE syndrome (Posterior fossa anomalies, Hemangioma, Arterial anomalies, Cardiac defects, Eye anomalies).
T. M. Morgan, J. M. Colazo, L. Duncan, R. Hamid, K. M. Joos   +4 more
doaj   +1 more source

Treatment of large cutaneous facial hemangioma with propranolol in a child with biliary atresia and esophageal varices

Caspian Journal of Pediatrics, 2017
Introduction:  Biliary atresia (BA) is the most common cause of neonatal jaundice, for which surgery is indicated. It may lead to portal hypertension and esophageal varices. Sometimes, BA is related to other congenital anomalies and malformation, while a
Mohammad Reza Esmaeili Dooki, Abbas Hadipour, Sanaz Mehrabani, Neda Joghtaei, Hajighorban Noreddini, Mehrangiz Amiri, Mohammadreza Salehiomran   +6 more
doaj  

The Quality of Life Impact of Vascular Anomalies on Patients and Their Families: Experience of a Tertiary Australian Centre

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim Chronic paediatric conditions often significantly impact the patients' and their families' quality of life (QoL). There is a paucity in the medical literature around the QoL impact of paediatric vascular anomalies on patients and their families in the Australian context. This study aims to address this gap.
Kwan Lam (Genevieve) Chow, Gloria Fong, Kelvin Truong, William Luu, Li‐Chuen Wong   +4 more
wiley   +1 more source

Nail Clubbing‐Associated With a Large Segmental Infantile Hemangioma of the Arm in a Patient With PHACES Syndrome

Pediatric Dermatology, EarlyView.
ABSTRACT Although infantile hemangiomas (IH) are common vascular tumors of childhood, associated nail abnormalities are rare. We report a child with a large segmental IH of the upper limb with marked, ipsilateral nail clubbing, which gradually improved until the age of 7 years.
Stefan Blunder, Lisa Weibel, Nicole Knöpfel, Martin Theiler, Agnes Schwieger‐Briel, Isabelle Luchsinger   +5 more
wiley   +1 more source

Early Intervention Effects and Risk Factors for Residual Skin Changes in Infantile Hemangiomas

The Journal of Dermatology, Volume 53, Issue 9, Page 1296-1304, September 2026.
ABSTRACT Infantile hemangioma (IH) characteristically progresses through proliferative, involuting, and involuted phases, and typically undergoes spontaneous regression after the age of five. Therefore, the traditional management strategy has been based on a “wait‐and‐see policy”.
Kayoko Okuda, Motoki Nakamura, Reiko Nakamura, Sachiyo Takagi, Akimichi Morita   +4 more
wiley   +1 more source

Exploratory Analysis of the Inhibitory Effects of Propranolol on NLRP3 and Pyrin Inflammasomes

ACR Open Rheumatology, Volume 8, Issue 8, August 2026.
Objective Propranolol, a nonselective beta receptor blocking agents, impacts cAMP levels and is commonly used to treat hypertension and hemangioma in children and adults. Although there are reports indicating its anti‐inflammatory properties, the exact mechanism is not fully understood. Methods Murine and human monocytes and macrophages were exposed to
Renske J. de Jong, Christopher T. Neullens, Aljoscha Swoboda, Melanie Saers, Philipp Berger, Sudheendra Hebbar Subramanyam, Anastasia Wiener, Kim Ohl, Ralf Weiskirchen, Heidi Noels, Tilmann Kallinich, Julia Guthrie, Christoph Kessel, Klaus Tenbrock   +13 more
wiley   +1 more source