منابع مشابه
Spontaneous Coronary Artery Dissection: A Rare Manifestation of Alport Syndrome
Alport syndrome (AS) is a genetic disorder due to inheritance of genetic mutations which lead to production of abnormal type IV collagen. AS has been associated with renal, auditory, and ocular diseases due to the presence of abnormal alpha chains of type IV collagen in the glomerulus, cochlea, cornea, lens, and retina. The resulting disorder includes hereditary nephritis, corneal opacities, an...
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Background: Osteopoikilosis (OPK) is a rare inherited condition of the bones, transmitted as an autosomal dominant trait characterized by numerous hyperostotic areas that tend to localize in periarticular osseous regions. It is usually asymptomatic and is often diagnosed incidentally during x-rays made by other reasons. We present a case of 34-year-old man suffering from polyarthralgia an...
متن کاملOrtner’s Syndrome-A Rare Cause of Hoarseness: Its Importance to an Otorhinolaryngologist
Introduction: Cardiovocal hoarseness (Ortner’s syndrome) is hoarseness of voice due to recurrent laryngeal nerve involvement secondary to cardiovascular disease. Recurrent laryngeal nerve in its course (especially the left side) follows a path that brings it in close proximity to numerous structures. These structures interfere with its function by pressure or by disruption of the nerve caused b...
متن کاملA rare cause of a piriformis syndrome.
BACKGROUND AND OBJECTIVE A less common but important cause of buttock and leg pain known as "Piriformis Syndrome". Piriformis syndrome is all intrinsic pathology of the piriformis itself, such as myofascial pain, anatomical variations, hypertrophy, and myositis ossificans or it is caused by trauma to the pelvis or buttock. In this case report we are going to present a rare cause of piriformis s...
متن کاملdyke-davidoff-masson syndrome- a rare cause of refractory epilepsy.
dyke-davidoff-masson syndrome (ddms) is a syndrome associated with refractory epilepsy. ddms is a rare syndrome characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation. the characteristic radiologic features are cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. the case was an 18 years old female with seizures, hemiparesis of the ri...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2014
ISSN: 1757-790X
DOI: 10.1136/bcr-2013-201731