Results 61 to 70 of about 6,705 (199)
Multidisciplinary Oral Rehabilitation in Osteogenesis Imperfecta: 18‐Year‐Old Case Report
ABSTRACT Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder characterized by bone fragility and Type I collagen defects. Although dentinogenesis imperfecta (DI) is a classic manifestation, patients with OI may experience significant dental deterioration even in its absence due to inherent dentinal weakness.
Pegah Mosannen Mozafari +3 more
wiley +1 more source
Duas formas de apresentação da amiloidose em ORL
Objectivo: Apresentação de dois casos clínicos de amiloidose com apresentação em ORL, assim como uma revisão teórica sobre esta patologia, nomeadamente a forma de apresentação clínica, diagnóstico e opções terapêuticas.
Maria Inês Silva +6 more
doaj +1 more source
Infantile Epileptic Spasms Syndrome Complicating Mosaic Down‐Turner Syndrome: A Case Report
ABSTRACT Severe baseline developmental delays in complex genetic syndromes like Down‐Turner mosaicism can completely mask the psychomotor regression of Infantile Epileptic Spasms Syndrome (IESS). Clinicians must maintain a high index of suspicion and prioritize early video‐EEG screening for any abnormal paroxysmal movements.
Mohammad Shahrori +4 more
wiley +1 more source
MANAGEMENT AND ROUTING OF CHILDREN WITH SYNDROMAL MACROGLOSSIA
The issue of management problems and substantiation of a multidisciplinary approach to the rehabilita-tion of patients with macroglossia by involving specialists of various profiles in all periods of development re-quires careful analysis and ...
A.O. Melnyk +4 more
doaj +1 more source
ABSTRACT Aims Acromegaly is a chronic, progressive disease characterised by excess growth hormone secretion and elevated circulating insulin‐like growth factor 1 levels. Data on hepatic fat content and liver stiffness in adults with active or controlled acromegaly remain inconsistent.
Alessandro Mantovani +8 more
wiley +1 more source
Alpha‐Mannosidosis in a 3.5‐Year‐Old Girl: A Case Report
ABSTRACT Alpha‐mannosidosis is a rare lysosomal storage disease caused by a deficiency of the enzyme alpha‐mannosidase. It manifests as a continuous spectrum of signs and symptoms characterized by dysmorphic features, skeletal abnormalities, delayed psychomotor and speech development, impaired hearing, and psychiatric involvement. When suspected, alpha‐
Samuel Bonilla Fornes +4 more
wiley +1 more source
Anterior tongue reduction surgery for paediatric macroglossia
Objective:Anterior tongue reduction is indicated when macroglossia causes problems with oral hygiene, airway compromise, deglutition, articulation or orthognathic complications.
R Hewitt +4 more
core +1 more source
Partial glossectomy as an auxiliary method to orthodontic treatment of dentofacial deformity
Summary Introduction: macroglossia is a condition which influences the size and shape of the teeth employed due to the forces on teeth. Objective: To establish bases for the indication of partial glossectomy associated with ...
Fued Samir Salmen +1 more
doaj +1 more source
ABSTRACT Objectives This study compares postoperative outcomes of transoral robotic surgery (TORS) and traditional lingual tonsillectomy in pediatric patients with persistent obstructive sleep apnea (OSA) following tonsillectomy and adenoidectomy (T&A).
Mona Dabbas +5 more
wiley +1 more source
Macroglossia is defined as an abnormal enlargement of the tongue that predominantly affects pediatric patients and is not frequent in adult patients. Hypothyroidism and hyperpituitarism may cause macroglossia in adults.
Kiichi Hirota
core +1 more source

