Results 301 to 310 of about 418,967 (342)
Some of the next articles are maybe not open access.
New England Journal of Medicine, 2004
The most common clinical manifestations of fibromuscular dysplasia (FMD) are hypertension due to renal artery involvement and transient ischemic attack or stroke due to carotid or vertebral artery involvement. Patients with renal artery FMD and hypertension should undergo primary angioplasty with the goal of curing the hypertension.
David P, Slovut, Jeffrey W, Olin
openaire +3 more sources
The most common clinical manifestations of fibromuscular dysplasia (FMD) are hypertension due to renal artery involvement and transient ischemic attack or stroke due to carotid or vertebral artery involvement. Patients with renal artery FMD and hypertension should undergo primary angioplasty with the goal of curing the hypertension.
David P, Slovut, Jeffrey W, Olin
openaire +3 more sources
Pediatric Anesthesia, 2021
AbstractBronchopulmonary dysplasia is the most frequent adverse outcome of prematurity. Before implementation of antenatal steroids and surfactant therapy, bronchopulmonary dysplasia was mostly characterized by fibrotic, scarred, and hyper‐inflated lungs due to pulmonary injury following mechanical ventilation and oxygen toxicity.
Alexander R. Schmidt +1 more
openaire +2 more sources
AbstractBronchopulmonary dysplasia is the most frequent adverse outcome of prematurity. Before implementation of antenatal steroids and surfactant therapy, bronchopulmonary dysplasia was mostly characterized by fibrotic, scarred, and hyper‐inflated lungs due to pulmonary injury following mechanical ventilation and oxygen toxicity.
Alexander R. Schmidt +1 more
openaire +2 more sources
Acrofacial dysplasia resembling geleophysic dysplasia
American Journal of Medical Genetics, 1984AbstractWe report on a 12‐year‐old girl with acrofacial dysplasia, growth retardation, joint contractures, mitral valve incompetence and focal hepatic storage of material reacting histochemically as glycoprotein. The patient's phenotype resembles that of patients with geleophysic dysplasia but differs with respect to facial appearance, milder changes ...
J, Spranger +4 more
openaire +2 more sources
METAPHYSEAL DYSPLASIA, EPIPHYSEAL DYSPLASIA, DIAPHYSEAL DYSPLASIA, AND RELATED CONDITIONS
A.M.A. Archives of Internal Medicine, 1954PROGRESSIVE diaphyseal dysplasia, so-named by Neuhauser, Schwachman, Wittenborg, and Cohen, in 1948,8is also known as Engelmann's disease.* Fairbank6believes that Cockayne4described the first case in 1920 and mentions the other few reports of the syndrome. Affected patients are weak and thin and are shorter than normal in stature.
W P, JACKSON, J, HANELIN, F, ALBRIGHT
openaire +2 more sources
Journal of the American Academy of Dermatology, 2007
Digitocutaneous dysplasia is a rare X-linked dominant genetic syndrome characterized by multiple digital fibromas, atrophic plaques, dental anomalies, dysmorphic features, and bone anomalies. We report the case of a 2-year-old Mexican girl with this rare condition and discuss the clinical, histologic, and genetic features.
Arash, Izadpanah +4 more
openaire +2 more sources
Digitocutaneous dysplasia is a rare X-linked dominant genetic syndrome characterized by multiple digital fibromas, atrophic plaques, dental anomalies, dysmorphic features, and bone anomalies. We report the case of a 2-year-old Mexican girl with this rare condition and discuss the clinical, histologic, and genetic features.
Arash, Izadpanah +4 more
openaire +2 more sources
Hormone Research in Paediatrics, 2002
<i>Definition:</i> Fibrous dysplasia (FD) of bone is a non-inheritable congenital disorder affecting both genders. It is characterized by expanding fibrous lesions, which contain bone-forming mesenchymal cells. <i>Pathophysiology:</i> FD is caused by a somatic activating mutation of the alpha subunit of the Gs protein (Gsα ...
Eckhard, Schoenau, Frank, Rauch
openaire +2 more sources
<i>Definition:</i> Fibrous dysplasia (FD) of bone is a non-inheritable congenital disorder affecting both genders. It is characterized by expanding fibrous lesions, which contain bone-forming mesenchymal cells. <i>Pathophysiology:</i> FD is caused by a somatic activating mutation of the alpha subunit of the Gs protein (Gsα ...
Eckhard, Schoenau, Frank, Rauch
openaire +2 more sources
Acta Oto-Laryngologica, 2005
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the ...
Young Ho, Kim +3 more
openaire +2 more sources
Craniometaphyseal dysplasia is a rare bone disorder of unknown etiology characterized by overgrowth of the skull base or craniofacial bones and abnormal remodeling of the metaphyses of the long bones. We present a sporadic case of craniometaphyseal dysplasia associated with facial paralysis observed in a 4-year-old female, which emphasizes the ...
Young Ho, Kim +3 more
openaire +2 more sources
Orbit, 2010
An atypical presentation of fibrous dysplasia with a very large cystic component is described. The MR pattern was not diagnostic.
Devron H, Char +3 more
openaire +2 more sources
An atypical presentation of fibrous dysplasia with a very large cystic component is described. The MR pattern was not diagnostic.
Devron H, Char +3 more
openaire +2 more sources