Results 41 to 50 of about 4,403,070 (230)

Development and Validation of the Expectations of Aesthetic Rhinoplasty Scale

open access: yesArchives of Plastic Surgery, 2016
Background There is a growing concern in the field of aesthetic surgery about the need to measure patients' expectations preoperatively. The present study was designed to develop and validate the Expectations of Aesthetic Rhinoplasty Scale (EARS), and ...
Mohsen Naraghi, Mohammad Atari
doaj   +1 more source

Exploring the relationship between self-compassion and body dysmorphic symptoms in adolescents

open access: yes, 2020
Current cognitive and behavioural models of body dysmorphic disorder aetiology highlight a possible role of deficits in self-compassion as a vulnerability factor. Yet, there has been little empirical research on the role of self-compassion in adolescents'
Zimmer-Gembeck, Melanie J   +3 more
core   +1 more source

Self‐discrepancy in body dysmorphic disorder [PDF]

open access: yesBritish Journal of Clinical Psychology, 2003
Objectives: According to self‐discrepancy theory (SDT), depression, social anxiety, eating disorders and paranoia result from different types of conflicting self‐beliefs. Body dysmorphic disorder (BDD) consists of a preoccupation with imagined or slight defects in one's appearance, which is often associated with a depressed mood and social anxiety. SDT
Veale, David   +3 more
openaire   +4 more sources

Body dysmorphic disorder and depression among male undergraduate students in a Malaysian University

open access: yesFrontiers in Psychiatry, 2022
IntroductionBody dysmorphic disorder (BDD) and depression have been reported to be both prevalent among young people worldwide, resulting in serious implications in their quality of life and social functioning.
Waye Hann Kang   +6 more
doaj   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston   +6 more
wiley   +1 more source

Suicide and Suicidality in Children and Adolescents with Chronic Skin Disorders: A Systematic Review

open access: yesActa Dermato-Venereologica, 2023
Suicide in young children is rare; the incidence increases towards the end of adolescence. Skin disorders confer a high prevalence of psychiatric and psycho­logical comorbidities.
Richard Barlow   +9 more
doaj   +1 more source

Musculoskeletal Phenotypes of 19 Patients With X‐Linked HNRNPH2‐Related Neurodevelopmental Disorder: A Prospective Case Series

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Detailed clinical phenotypes have been previously reported for 33 individuals with X‐linked HNRNPH2‐related neurodevelopmental disorder. Of these, 75% self‐reported a musculoskeletal abnormality, including hip dysplasia, scoliosis, kyphosis, lordosis, pes planus, arthritis, and missing spinous processes.
Ambar Garcia   +6 more
wiley   +1 more source

Body Dysmorphic Disorder: a Comprehensive Review

open access: yes, 2021
Body dysmorphic disorder is psychiatric morbidity that comes under the spectrum of obsessive-compulsive disorders. Individuals suffering from body dys- morphic disorder are incredibly concerned about their minor or so-called defects to such an extent ...
Nasim, Sundus   +4 more
core   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

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