Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Diaphyseal sclerosis"'
Publikováno v:
BMJ case reports. 14(10)
Establishing the cause of unilateral leg pain is difficult in the settings of tibial diaphyseal sclerosis. This patient, a 36-year-old woman presented with unilateral pretibial leg pain for past 7 months without history of trauma, infections, systemi
Akademický článek
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Autor:
Ghada A. Otaify, Marina Stolina, Marwan Shinawi, Olivier Lichtarge, Abby S. Hollander, Wei-Shen Chen, Samir K. El-Mofty, J. Eric Gordon, Albert S. Woo, Gary S. Gottesman, Michael P. Whyte, Marisa V. Andrews, William H. McAlister, Panagiotis Katsonis, Fan Zhang, Deborah V. Veis
Publikováno v:
Bone. 107:161-171
Gnathodiaphyseal dysplasia (GDD; OMIM #166260) is an ultra-rare autosomal dominant disorder caused by heterozygous mutation in the anoctamin 5 (ANO5) gene and features fibro-osseous lesions of the jawbones, bone fragility with recurrent fractures, an
Publikováno v:
Medicine
Rationale: Multiple diaphyseal sclerosis (MDS), known as Ribbing disease, is a rare congenital bone disease resulting from autosomal recessive inheritance. The case study involved a 22-year-old female patient who had been diagnosed with chronic scler
Publikováno v:
Acta Radiologica, 59(4), 448-453
BackgroundRibbing disease, or multiple diaphyseal sclerosis, is a rare benign bone dysplasia.PurposeTo systematically review the literature to determine the clinical and radiological presentation of patients with Ribbing disease as well as the effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e3422c0f6b500c75098bc64ab971d06
https://doi.org/10.1177/0284185117719575
https://doi.org/10.1177/0284185117719575
Publikováno v:
Europe PubMed Central
Sclerosing bone disorders are uncommon diseases and represent a diagnostic challenge. Osteocondensation is a bone alteration, involving both acquired and hereditary conditions. Multiple diaphyseal sclerosis (Ribbing disease) is an inherited condition
Publikováno v:
Calcified tissue international. 104(6)
Gnathodiaphyseal dysplasia (GDD; OMIM#166260) is a rare skeletal disorder which is mainly characterized by cemento-osseous lesions in mandibles, bone fragility, bowing and diaphyseal sclerosis of tubular bones. GDD is caused by point mutations in Ano
Publikováno v:
JBJS case connector. 8(2)
Case We review the case of a 44-year-old man with Camurati-Engelmann disease, who presented with chronic right hip pain that did not improve following intra-articular hip injections. He was functionally debilitated because of the worsening pain. Rout
Publikováno v:
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons. 74(12)
Gnathodiaphyseal dysplasia (GDD) is a rare hereditary syndrome characterized by cemento-ossifying fibromas of the maxillary bones, fragile bones, curvature and cortical thinning of the tubular bones, and diaphyseal sclerosis of the long bones. In thi
Publikováno v:
Journal of Orthopaedic Science. 16:828-831
Ribbing disease is a rare condition of diaphyseal sclerosis first described by Ribbing [1], characterized by benign endosteal and periosteal bone growth confined to the diaphyses of the long bones in young adults, usually limited to the lower extremi