Results 191 to 200 of about 5,144,883 (382)

Age at diagnosis of paediatric unilateral and bilateral permanent hearing loss in Eastern Switzerland: a retrospective cohort study

open access: yesSwiss Medical Weekly
STUDY AIM: Undiagnosed and therefore untreated permanent paediatric hearing loss can have a detrimental impact on a child’s speech, language, social and educational development, and quality of life.
Samuel P. Hofmann   +2 more
doaj   +1 more source

Hearing loss and COVID-19: A note

open access: yesAmerican Journal of Otolaryngology, 2020
W. Sriwijitalai, V. Wiwanitkit
semanticscholar   +1 more source

Stress, Health, and Injury Among Illinois Farmers

open access: yesAmerican Journal of Industrial Medicine, EarlyView.
ABSTRACT Objectives The goal of this cross‐sectional study was to characterize stress, injury, and chronic health conditions among agricultural producers in Illinois. The objectives were to: (1) describe the prevalence and nature of work‐related injuries; (2) describe chronic health conditions, stress, and symptoms of mental health conditions; and (3 ...
Josie M. Rudolphi   +3 more
wiley   +1 more source

Hearing loss in children with neurodevelopmental or genetic disorders visiting a phoniatric clinic at a tertiary hospital in Cairo

open access: yesThe Egyptian Journal of Otolaryngology
Background Children with special needs often manifest multiple developmental, linguistic, cognitive, and behavioral symptoms. Hearing difficulties could be sometimes misdiagnosed, aggravating the behavioral manifestations and possibly affecting their ...
Heba Tallah Sherif Abd El Hady   +1 more
doaj   +1 more source

Phenotypic Characterization of Seven Pediatric Patients Diagnosed With KAT6B‐Related Disorders: Case Series and Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genitopatellar syndrome (GPS) and Say‐Barber‐Biesecker‐Young‐Simpson Syndrome (SBBYSS) are clinically distinct neurodevelopmental disorders caused by monoallelic pathogenic variants in KAT6B. In some cases, GPS and SBBYSS features can overlap, determining an intermediate phenotype.
Vittorio Maglione   +12 more
wiley   +1 more source

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio   +13 more
wiley   +1 more source

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