RESUMEN
METHODOLOGY: An electronic search was done in PUBMED, SCOPUS, and a hand search was done in radiology, periodontology, and oral surgery journals. The search yielded 428 results, from which only 6 articles were selected for this literature review. Both prospective and retrospective studies were included. Clinical studies with information on the pre-implant condition of the site, detailed implant procedure, and follow-up after implant placement of more than 6 months were only considered for this review. RESULTS AND CONCLUSION: Limited clinical studies, shorter follow-up periods were the shortcomings of this review. However, it can be summarized that dental implants should not be placed at the site of FCOD, however can be placed at adjacent sites. Variations in implant type or the implant length had no bearing on the survival of implants at the sites of FCOD.
Asunto(s)
Implantes Dentales , Humanos , Osteomielitis/cirugía , Implantación Dental/métodos , Displasia Fibrosa Ósea/cirugíaRESUMEN
An increased level of ammonia in the bloodstream, or hyperammonemia, is a symptom associated with metabolic disorders referred to as inborn errors of metabolism. Urea cycle disorder is a congenital abnormality or absence of one of the six enzymes involved in the elimination of ammonia. Administration of certain medications, high protein diet, excessive exercise, surgical procedures, or trauma can precipitate symptoms of mental confusion, seizure-like activity, and ataxia. This paper reviews the literature with insight into current treatment and management options of the disorder and modification of treatment for the dental patient.
Asunto(s)
Aciduria Argininosuccínica , Atención Dental para Enfermos Crónicos , Enfermedades de la Boca/etiología , Preparaciones Farmacéuticas Odontológicas/efectos adversos , Aciduria Argininosuccínica/complicaciones , Aciduria Argininosuccínica/enzimología , Aciduria Argininosuccínica/patología , Citocromo P-450 CYP3A/metabolismo , Interacciones Farmacológicas , Humanos , Hiperamonemia/complicaciones , Enfermedades de la Boca/terapiaRESUMEN
Philosophical theory about the nature of human beings has far reaching consequences on our understanding of various issues faced by them. Once taken as self-evident, it becomes the foundation on which knowledge gets built. The cause of concern is that this theoretical framework rarely gets questioned despite its inherent limitations and self-defeating consequences, leading to crisis in the concerned field. The field, which is facing crisis today, is that of medicine, and the paradigmatic stance that is responsible for the crisis is Cartesian dualism-a view that mind and body are essentially separate entities. This paper discusses Cartesian dualism in the context of the practice of medicine. Focusing more closely on how disease, health and treatment are defined through this position, the paper builds up its critique by throwing light on its accomplishments, limitations and self-defeating consequences. The paper also seeks to understand why this dualism is still alive despite its disavowal from philosophers, health practitioners and lay people.
RESUMEN
We report a case of a 42-year-old female who was referred to our department for the management of a fractured dental needle following administration of an inferior alveolar nerve block. The fractured needle was successfully removed under general anaesthesia. We also suggest some guidelines for preventing this unfortunate event.
Asunto(s)
Anestesia Dental/instrumentación , Nervio Mandibular , Agujas/efectos adversos , Bloqueo Nervioso/instrumentación , Adulto , Anestesia Dental/efectos adversos , Anestesia Endotraqueal , Falla de Equipo , Femenino , Cuerpos Extraños/etiología , Cuerpos Extraños/cirugía , Migración de Cuerpo Extraño/cirugía , Humanos , Cóndilo Mandibular , Bloqueo Nervioso/efectos adversos , Músculos PterigoideosRESUMEN
We report a family of three siblings with Childhood Ataxia with Cerebral Hypomyelination. All the siblings presented with early onset cerebellar ataxia beginning around five years of age with mild mental retardation. MRI showed diffuse white matter signal changes in all three patients with cerebellar atrophy while the spectroscopy was abnormal only in the eldest who was the most severely affected. The cases are reported for their rarity as well as for an opportunity of observing this uncommon disease in its stages of evolution in three siblings.