Results 291 to 300 of about 513,093 (363)
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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
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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
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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
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Head and Neck, 2019
Potentially malignant disorders of the oral cavity (OPMD) are a heterogeneous group of lesions associated with a variable risk of malignant transformation (MT) to invasive cancer.
O. Iocca +9 more
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Potentially malignant disorders of the oral cavity (OPMD) are a heterogeneous group of lesions associated with a variable risk of malignant transformation (MT) to invasive cancer.
O. Iocca +9 more
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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
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<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
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BJOG: an International Journal of Obstetrics and Gynaecology, 2019
Persistent infection with high‐risk human papillomavirus can lead to cervical dysplasia and cancer. Recent studies have suggested associations between the composition of the vaginal microbiota, infection with human papillomavirus (HPV) and progression to
Johanna Norenhag +5 more
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Persistent infection with high‐risk human papillomavirus can lead to cervical dysplasia and cancer. Recent studies have suggested associations between the composition of the vaginal microbiota, infection with human papillomavirus (HPV) and progression to
Johanna Norenhag +5 more
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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
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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
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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
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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
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Clinics in Chest Medicine
Bronchopulmonary dysplasia (BPD) is a chronic lung disease, associated with premature birth, that arises during the infantile period. It is an evolving disease process with an unchanged incidence due to advancements in neonatal care which allow for the survival of premature infants of lower gestational ages and birth weights.
Katelyn G, Enzer +2 more
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Bronchopulmonary dysplasia (BPD) is a chronic lung disease, associated with premature birth, that arises during the infantile period. It is an evolving disease process with an unchanged incidence due to advancements in neonatal care which allow for the survival of premature infants of lower gestational ages and birth weights.
Katelyn G, Enzer +2 more
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Developmental Dysplasia of the Hip
Pediatrics, 2018The evaluation and treatment of hip dysplasia continues to evolve. In this article, we review recent advances in the management of hip dysplasia. Pediatricians are often the first to identify developmental dysplasia of the hip (DDH) and direct subsequent
Scott Yang +3 more
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Journal of the American Academy of Orthopaedic Surgeons, 2004
Fibrous dysplasia is a developmental disorder of bone that can present in a monostotic or polyostotic form. Primarily affecting adolescents and young adults, it accounts for 7% of benign bone tumors. Many of the asymptomatic lesions are found incidentally; the remainder present with symptoms of swelling, deformity, or pain.
Selene G, Parekh +3 more
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Fibrous dysplasia is a developmental disorder of bone that can present in a monostotic or polyostotic form. Primarily affecting adolescents and young adults, it accounts for 7% of benign bone tumors. Many of the asymptomatic lesions are found incidentally; the remainder present with symptoms of swelling, deformity, or pain.
Selene G, Parekh +3 more
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