Results 211 to 220 of about 682,435 (246)

Artificial Intelligence in Neonatal Care: The Breadth of Promise, the Depth of Challenge—An Overview

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Artificial intelligence (AI) is becoming an integral tool in clinical care. The recent position statement by the Royal Australasian College of Physicians (RACP) provides a timely practical blueprint on implementing and monitoring the use of AI in clinical practice.
N. M. Lai, K. T. Yeo, J. Y. Kong, M. E. Abdel‐Latif   +3 more
wiley   +1 more source

Use of Telehealth Technology in the Delivery of Community Health Services for Children and Young People in New Zealand. A Scoping Review

Journal of Paediatrics and Child Health, EarlyView.
ABSTRACT Aim To explore what is known about the use of telehealth for delivering community health services to children and young people in New Zealand, this review will map the existing evidence and identify key characteristics, gaps, and opportunities to support equitable service delivery.
S. Williams, J. Gardiner, T. W. Barbarich‐Unasa, J. Blamires   +3 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

Atrophic Papulosis: A Systematic Review of Pediatric Cases

Pediatric Dermatology, EarlyView.
ABSTRACT Background Atrophic papulosis is a rare occlusive vasculopathy that can present with isolated cutaneous disease or with systemic involvement. Pediatric cases are uncommon, and existing reports are heterogeneous, limiting understanding of disease patterns, timing of organ involvement, and outcomes.
Ou Jia Emilie Wang, Alennie Lopez, Renee Gabrielle Fajardo, Richard I. Crawford, Joseph M. Lam   +4 more
wiley   +1 more source

Interim Update on Reactive Infectious Mucocutaneous Eruption (RIME)

Pediatric Dermatology, EarlyView.
ABSTRACT Reactive infectious mucocutaneous eruption (RIME), a term describing blistering skin and mucosal lesions, is a term coined by a group of Pediatric Dermatology Research Alliance (PeDRA) researchers and first published in 2021. Since that time, the literature has grown with reports of diverse infectious triggers, management strategies, and ...
Michele Ramien, Yvonne E. Chiu, Sarah D. Cipriano, Sadaf Hussain, A. Yasmine Kirkorian, Minnelly Luu, Erin F. Mathes, Vikash S. Oza, Martin Theiler, James R. Treat, Patrick M. Meyer Sauteur, Irene Lara‐Corrales   +11 more
wiley   +1 more source

Operative Management of Phakomatosis Pigmentokeratotica Sequelae: Surgical Techniques and Procedural Pearls

Pediatric Dermatology, EarlyView.
ABSTRACT Phakomatosis pigmentokeratotica (PPK) is a rare variant of epidermal nevus syndrome, classically characterized by the coexistence of nevus sebaceus and nevus spilus. Secondary neoplasms arising within nevus sebaceus, including syringocystadenoma papilliferum (SPAP), can cause persistent irritation, discomfort, and bleeding that negatively ...
Helen Chen, Brooke Walterscheid, Michelle Tarbox, Alba Posligua   +3 more
wiley   +1 more source

Clinicogenetic Characterization of H Syndrome in a South African Child

Pediatric Dermatology, EarlyView.
ABSTRACT H syndrome is a rare autosomal recessive genodermatosis caused by loss‐of‐function SLC29A3 variants, combining hyperpigmented indurated plaques and hypertrichosis with life‐threatening autoinflammation. We report a 5‐year‐old South African girl of first‐cousin parents who presented with hyperinflammation mimicking macrophage activation ...
Tshimogo Tswelopele Sathekge, Claude Bailly   +1 more
wiley   +1 more source

A PIGG congenital disorder of glycosylation (PIGG‐CDG) variant associated with an Emm− red blood cell phenotype in a pediatric patient

Transfusion, EarlyView.
Abstract Background The high‐prevalence Emm antigen is an epitope on the GPI (glycosylphosphatidylinositol) glycolipid backbone, which anchors proteins to the cell surface. Inherited loss‐of‐function of PIGG (or PIGO) results in the rare Emm− red cell (RBC) phenotype and is associated with congenital disorders of glycosylation (CDG).
Alastair Murray, Connie M. Westhoff, Sunitha Vege, Hallie Lee‐Stroka, Randall W. Velliquette, William J. Lane, Jillian G. Buchan, Nabiha H. Saifee, Rida A. Hasan   +8 more
wiley   +1 more source