Results 41 to 50 of about 11,914 (280)
Polyostotic Fibrous Dysplasia [PDF]
Summary A case of polyostotic fibrous dysplasia in a 5-year-old girl is reported. The diagnosis was made by the characteristic triad of predominantly unilateral bone lesions, precocious “puberty,” and unilateral skin pigmentation, and was substantiated by radiographic and pathologic examination of the bone lesions. The early onset of menses (second
Louis J. Hackett+1 more
openaire +6 more sources
Polyostotic fibrous dysplasia: imaging findings of a controversial case [PDF]
Fibrous dysplasia is a rare non-neoplastic tumor-like congenital bone disease that is most likely associated with GNAS gene mutations, with a broad spectrum of clinical presentations, ranging from isolated monostotic and polyostotic forms to other extra ...
Francesca De Michele+3 more
doaj +1 more source
A Rare Case of Polyostotic Fibrous Dysplasia
This case repost discusses clinical and biochemical features of polyostotic fibrous dysplasia, a rare entity which leads to significant morbidity and multisystem manifestation in children.The diagnosis ,differentials, treatment and complications are ...
Sugha Varuna, Bharti Sapna
semanticscholar +1 more source
Dental implantology and fibrous dysplasia: A 6‐year follow‐up case report and a literature review
Abstract Background and Aim It is unclear if fibrous dysplasia (FD) represents a contraindication for implant borne rehabilitation, and only two successful cases are reported in the literature with a 4–2‐year follow‐up. The present paper discusses this issue reporting a full‐arch maxillary rehabilitation with a >5‐year follow‐up.
Giuseppe Lizio+4 more
wiley +1 more source
Jaffe Lichtenstein Type Polyostotic Fibrous Dysplasia with Unilateral Absent Testis [PDF]
Fibrous dysplasias are developmental bone disorders in which the medullary cavity is replaced by fibrous tissue. It can be monostotic involving a single bone or polyostotic involving multiple bones.
Anand Ramakrishnan+3 more
doaj +1 more source
ABSTRACT This study aimed to evaluate the prevalence of and risk factors for coxa vara deformity in patients with fibrous dysplasia/McCune‐Albright syndrome (FD/MAS). This study was conducted at the National Institutes of Health and Leiden University Medical Center. All patients with any subtype of FD/MAS, FD involving the proximal femur, one or more X‐
Maartje E. Meier+7 more
wiley +1 more source
Post-COVID-19 Exacerbation of a Stable Fibrous Dysplasia: A Case Report. [PDF]
ABSTRACT Fibrous dysplasia (FD) is a rare, benign fibro‐osseous lesion characterized by replacement of normal bone with extensive fibrous stroma due to abnormalities in osteoblast differentiation. After puberty and during adulthood, FD lesions usually become quiescent. However, some cases show signs of regrowth and reactivation.
Fatih MT+7 more
europepmc +2 more sources
Nosology of genetic skeletal disorders: 2023 revision
Abstract The “Nosology of genetic skeletal disorders” has undergone its 11th revision and now contains 771 entries associated with 552 genes reflecting advances in molecular delineation of new disorders thanks to advances in DNA sequencing technology.
Sheila Unger+20 more
wiley +1 more source
Osteocyte (OCY)‐specific degradation‐resistant HIF‐2α (HIF‐2α cDR) mice generated a high bone mass skeletal phenotype with increased trabecular bone and decreased cortical bone. Distal femoral metaphysis of HIF‐2α cDR mice showed evidence of bone marrow stromal tissue expansion, increased trabecular bone and new bone formation compared to cre‐negative ...
Sarah V. Mendoza+6 more
wiley +1 more source
Preliminary Results of Bone Lengthening over Telescopic Titanium Intramedullary Rod
Background. Limb lengthening and deformity correction in patients with abnormal bone associating fragility often require an approach combining methods of external and internal fixation. This study demonstrates results of simultaneous application of external fixator, and telescopic rod for femoral lengthening and deformity correction in three children ...
Eduard Mingazov+5 more
wiley +1 more source