نتایج جستجو برای: mouth abnormalities
تعداد نتایج: 136693 فیلتر نتایج به سال:
to report the oral findings, including dental anomalies, ectopic eruption of the maxillary permanent first molars and periodontal disease and soft tissue alterations, in a subject with apert syndrome. clinical and radiographic examination of a patient with apert syndrome, aged 21 years old, not previously submitted for orthodontic or orthognathic treatment. dental anomalies were present in a pa...
OBJECTIVES This study aimed to investigate the magnetic resonance imaging (MRI) characteristics and clinical and MRI follow-up findings of patients with neurological complications of enterovirus 71-related hand, foot and mouth disease. METHODS Data were collected from 12 patients who developed neurological complications of enterovirus 71-related hand, foot, and mouth disease during an enterov...
S-J syndrome is a rare autosomal recessive disorder of short stature, blepharophimosis, puckerd mouth, myotonia, muscular weakness, pectus carinatum and stiff joints. Case report: first case: n.1. A boy aged 7 years. His main abnormalities included puckered lip, blephharophimosis, muscular hypertrophy and weakness, pectus carinatum, short stature, shoulder joint limitation and myopia. Myotonic ...
Little attention has been paid to the aspects of cardiac injury-related foot and mouth disease (FMD) in young animals. So, this research was conducted to evaluate the serum biomarkers and electrocardiographic (ECG) evidence of myocardial injury in the infected lambs with FMD. During an outbreak, 33 lambs with FMD and 11 healthy lambs were randomly enrolled. After blood sampling, ECGs were taken...
s-j syndrome is a rare autosomal recessive disorder of short stature, blepharophimosis, puckerd mouth, myotonia, muscular weakness, pectus carinatum and stiff joints. case report: first case: n.1. a boy aged 7 years. his main abnormalities included puckered lip, blephharophimosis, muscular hypertrophy and weakness, pectus carinatum, short stature, shoulder joint limitation and myopia. myotonic ...
Hemangiomas are tumors of blood vessels identified by rapid endothelial cell proliferation in early infancy followed by involution over time. All other abnormalities are malformations resulting from anomalous development of vascular plexuses. This lesion in the oral cavity is not common. Despite its benign origin and behaviour, it is always of clinical importance to the dental profession and re...
BACKGROUND Nail abnormalities in childhood are generally uncommon. Recently, onychomadesis is described as a rare, late complication of hand-foot-mouth disease, which is a viral illness commonly seen in the pediatric age group. It is therefore important to elucidate the presentation of this entity, especially in the context of the hand-foot-mouth disease. CASE PRESENTATION We report a case of...
Laryngeal oedema, giving rise to stridor, is a recognized although rare complication following extubation of the trachea in children. It was our clinical impression that children with Down's syndrome, in particular, had a tendency to develop obstruction of the airway following operation. In Down's syndrome there are many abnormalities which affect the face and skull: those affect' ing the airwa...
Abstract Aim Electrolyte abnormalities are a common and serious consequence of nutritional deficiencies when patients nil-by-mouth. Timely intervention with multidisciplinary approach is known to improve outcome. This audit aimed assess adequacy initial electrolyte management timing dietetics referral in acute surgical requiring total parenteral nutrition university hospital. Method A retrospec...
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