Results 231 to 240 of about 218,477 (331)

Quality of life in children with unilateral hearing loss undergoing cochlear implantation: A systematic review and meta-analysis. [PDF]

open access: yesBraz J Otorhinolaryngol
Piva de Freitas P   +4 more
europepmc   +1 more source

Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

open access: yesPediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala   +9 more
wiley   +1 more source

Sensorineural deafness in a child with Prader-Willi Syndrome-A rare case report. [PDF]

open access: yesJ Family Med Prim Care
Saikrishna P   +5 more
europepmc   +1 more source

Academic achievement of children with unilateral or mild bilateral hearing loss: A systematic review

open access: yesReview of Education, Volume 13, Issue 2, August 2025.
Abstract There has been significant research on the association between hearing loss and academic achievement. However, many studies do not disaggregate by degree of hearing loss. Therefore, the risks to school performance posed by unilateral and mild bilateral hearing loss are not well understood, despite prevalence studies suggesting that 2.4 to 23 ...
Katherine Collier
wiley   +1 more source

Granulomatosis with polyangiitis presenting as isolated ear involvement: a case series and literature review. [PDF]

open access: yesActa Otorhinolaryngol Ital
Zorzi S   +8 more
europepmc   +1 more source

The Natural Course of Bosch‐Boonstra‐Schaaf Optic Atrophy Syndrome

open access: yesClinical Genetics, Volume 108, Issue 2, Page 168-178, August 2025.
Here, we present data on genetic variants and phenotype development of 47 individuals with Bosch‐Boonstra‐Schaaf optic atrophy syndrome, a rare neurodevelopmental disorder, highlighting the fact that the disease does not appear to be fundamentally progressive.
Ilia Valentin   +4 more
wiley   +1 more source

Microtia. [PDF]

open access: yesCMAJ
You P, Liu YC, Symonette C.
europepmc   +1 more source

Vitiligo

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 8, Page 968-987, August 2025.
Summary Vitiligo is a common pigment disorder of the skin resulting in destruction of melanocytes. Non‐segmental vitiligo (NSV) is an autoimmune disorder. The etiopathogenesis of segmental vitiligo (SV) remains incompletely understood. Genetic predisposition and increased vulnerability of melanocytes towards stressors lead to a melanocyte‐specific CD8+
Markus Böhm, Adrian Tanew
wiley   +1 more source

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