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osteogenesis imperfecta/obesità
Il collegamento viene salvato negli appunti
11 risultati
[Anesthetic management of an obese patient with osteogenesis imperfecta].
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Osteogenesis imperfecta (OI) is a rare hereditary disorder characterized by an excessive tendency to bone fractures and retarded growth, as well as variable involvement of other connective tissues such as teeth, sclerae, auditory bones and ligaments. A 30-year-old woman (body mass index of 39.6)
Spinal anesthesia in an obese patient with osteogenesis imperfecta.
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Weight loss surgery improves quality of life in pediatric patients with osteogenesis imperfecta.
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BACKGROUND
Osteogenesis imperfecta (OI) is an inherited disorder, which causes brittle bones resulting in recurrent fractures. The associated poor mobility of children with OI increases susceptibility to obesity, and obesity further dramatically limits mobility and increases fracture
Cross-sectional and longitudinal growth patterns in osteogenesis imperfecta: implications for clinical care.
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BACKGROUND
There is strikingly limited information on linear growth and weight in the different types of osteogenesis imperfecta (OI). Here, we define growth patterns further with the intent of implementing appropriate adaptations proactively.
METHODS
We report cross-sectional anthropometric data
Osteogenesis Imperfecta with Celiac Disease and Type II Diabetes Mellitus Associated: Improvement with a Gluten-Free Diet.
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Osteogenesis imperfecta (OI) is a genetic disease, with a connective tissue alteration, consisting in the presence of multiple spontaneous fractures or after minimal traumatism. Its association with other metabolic processes is rarely described. We present the clinical case of a female adult patient
[Osteogenesis imperfecta. Clinical, functional and multidisciplinary evaluation of 65 patients].
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BACKGROUND
Osteogenesis Imperfecta (OI) is a genetic disease, in which the main clinical features are increased bone fragility, pathological fractures, blue sclera, dentinogenesis imperfecta and conductive or mixed hearing loss. Clinical variability is wide. Although there is no curative treatment,
Extreme complications of Fixion nail in treatment of long bone fractures.
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The authors present their experience related to extreme complications in treatment of diaphyseal fractures of the long bones with application of the Fixion expansion intramedullary nail in a total of 48 surgeries. We have encountered six (12.5%) extreme complications in the management of fractures
Calcium metabolism evaluated by 47Ca kinetics: estimation of dermal calcium loss.
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Seventy-seven calcium balance and 47Ca turnover studies were performed in normal volunteers (n = 15) and in patients with osteoporosis (n = 12), primary hyperparathyroidism (n = 8), osteogenesis imperfecta (n = 5), medullary carcinoma of the thyroid (n = 4), thyrotoxicosis (n = 2) and intestinal
Diagnosis and treatment of osteopenic fractures in children.
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Osteopenic fractures occur in children every day. At times the osteopenic nature of these fractures is painfully obvious, as in neurofibromatosis and osteogenesis imperfecta, while in many other situations overt osteopenia does not declare itself, such as in normal and obese children. Normal
Early Acid Suppression Therapy Exposure and Fracture in Young Children.
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BACKGROUND
Acid suppression therapy (AST), including proton pump inhibitors (PPIs) and histamine H2-receptor antagonists (H2RAs), is frequently prescribed to treat symptomatic gastroesophageal reflux in otherwise healthy infants. PPI use has been associatedZebrafish Models of Human Skeletal Disorders: Embryo and Adult Swimming Together.
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Danio rerio (zebrafish) is an elective model organism for the study of vertebrate development because of its high degree of homology with human genes and organs, including bone. Zebrafish embryos, because of the optical clarity, small size, and fast development, can be easily used in
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