Results 61 to 70 of about 4,886 (203)
ABSTRACT The Thai Transplantation Society developed these clinical practice guidelines to establish a comprehensive standard for immunosuppressive therapy in adult kidney transplantation. While rooted in evidence‐based medicine, the objective of this document extends beyond local application, serving as a practical model for low‐to‐middle‐income ...
Suwasin Udomkarnjananun +12 more
wiley +1 more source
Background Microtia is reported to be one of the most common congenital craniofacial malformations. Due to the complex etiology and the ethical barrier of embryonic study, the precise mechanisms of microtia remain unclear.
Wenbo Liu +6 more
doaj +1 more source
Association of Ear Anomaly Type and Sex Concordance with Microtia Occurrence
Introduction: Microtia is a congenital malformation of the auricle that leads to serious functional and psychosocial consequences. Familial factors, such as the types of auricular anomalies present in family members and sex concordance between affected ...
Putri Putra Rimba +6 more
doaj +1 more source
A Case Report of Congenital Microtia-Atresia
Background and Objectives: Microtia-atresia is a rare congenital anomaly, which characterized by a small, abnormally shaped auricle (microtia) accompanied with narrow, blocked or absent ear canal (atresia). Microtia can occur appear either as independent
Marzieh Alipour, Khalil Khashei
doaj
Sensorineural hearing loss resulting from microtia and aural atresia is rare due to different embryologic origins of the external and inner ear. Consequently, cochlear implants are seldom performed in patients with microtia and/or aural atresia.
Wei Li Neo +4 more
doaj +1 more source
Diagnosing and Treating Microtia [PDF]
Instructions for examining and diagnosing patients with microtia and an overview of reconstructive options. Virtual Mentor is a monthly bioethics journal published by the American Medical Association.
openaire +2 more sources
ABSTRACT Background Treacher Collins Syndrome (TCS) is an uncommon congenital disease of the craniofacial complex. While there are ‘classic’ facial manifestations of TCS, they present with a wide range of variability. Face2Gene (F2G) is a deep‐learning algorithm that can provide differential diagnoses of syndromes via analysis of 2‐dimensional facial ...
Jie Han Timothy Sng +2 more
wiley +1 more source
Key Genes Identified in Nonsyndromic Microtia by the Analysis of Transcriptomics and Proteomics
As one of the common birth defects worldwide, nonsyndromic microtia is a complex disease that results from interactions between environmental and genetic factors.
Jing Ma (24574) +8 more
core +2 more sources
ABSTRACT Early recognition of syndromic features by dental professionals can lead to timely diagnosis and intervention, especially when systemic anomalies have been overlooked. Preventive and individualized dental management, supported by behavioral guidance, can achieve long‐term stability even in medically complex patients, including those with ...
Nazanin Nasr +4 more
wiley +1 more source
Bibliometric Analysis of Microtia-Related Publications From 2006 to 2020
Objective: Microtia is a congenital auricular malformation with a hypoplastic external ear that ranges in severity from a slightly smaller auricle to complete the absence of the auricle.
Wei Wang MD +4 more
doaj +1 more source

