Results 31 to 40 of about 1,058,904 (200)

An activating variant in CTNNB1 is associated with a sclerosing bone dysplasia and adrenocortical neoplasia.

, 2019
Activating CTNNB1 variant in a sclerosing bone ...
Anne Ronan (7419812), David M. Markie (4950169), Ruby White (7419805), Philip B. Daniel (7419816), Hui Peng (7419719), Sam Connors (7419806), Zandra A. Jenkins (7419819), Matthew F. Hunter (7419809), Andreas Zankl (60186), Stephen P. Robertson (4950166)   +9 more
core   +1 more source

Bone: Fibrous dysplasia of the bone [PDF]

, 2001
Review on Bone: Fibrous dysplasia of the bone, with data on clinics, and the genes ...
Dal, Cin P
core   +1 more source

Case reports - Mixed sclerosing dysplasia of the bone associated with ovarian and skin problems

, 2005
The clinical, radiologic, histopathologic, and genetic features of a sclerosing bone dysplasia found in three members of a family are described. The bone disorder affected all metaphyseal-diaphyseal regions of all long bones, the skull, and three ...
Gunal, I, Taymaz, A, Karatosun, VASFİ AKINCI, Toylu, A, Degirmenci, B   +4 more
core   +1 more source

Osteopoikilosis in a patient with familial adenopolyposis : A case report

Radiology Case Reports
Osteopoikilosis, a sclerosing bone dysplasia, is an asymptomatic incidental finding characterised by multiple bone islands. Although it requires no treatment there can be diagnostic uncertainty as appearances can be similar to osteoblastic metastases or ...
Rashed Al-Khudairi, MBBS, Alexandros Maris, MD, MSc, Ahmed Blehadj, MD, Angelo V. Vasiliadis, MD, PhD   +3 more
doaj   +1 more source

Osteopoikilosis of the axial skeleton and pelvis: A rare cause of back pain

BLDE University Journal of Health Sciences, 2019
Osteopoikilosis (OPK) is an autosomal dominant and rare skeletal condition characterized by discrete ovoid or round, multiple radiodense lesions scattered predominantly in the appendicular skeleton.
Reddy Ravikanth, Kanagasabai Kamalasekar
doaj   +1 more source

Clinical characteristics and the influence of rs1800470 in patients with Camurati-Engelmann disease

Frontiers in Endocrinology, 2022
BackgroundCamurati-Engelmann disease (CED) is a sclerosing bone dysplasia caused by transforming growth factor β1 (TGFB1) gene variants.ObjectiveWe aim to summarize the clinical characteristics and the efficacy of glucocorticoids in 14 individuals with ...
Hanting Liang, Ruizhi Jiajue, Wenting Qi, Wei Liu, Yue Chi, Yan Jiang, Ou Wang, Mei Li, Xiaoping Xing, Weibo Xia   +9 more
doaj   +1 more source

Colorectal Cancer: Epidemiology, Risk Factors, Signaling Pathways, Clinical Features, Screening, Diagnosis, and Management

MedComm, Volume 7, Issue 10, October 2026.
Colorectal cancer is a heterogeneous, adaptive disease shaped by population‐level risk, genomic and epigenetic alterations, tumor ecosystem evolution, and treatment pressure. This review integrates epidemiology, risk factors, signaling networks, clinical presentation, screening, molecular diagnosis, and stage‐ and biomarker‐guided management while ...
Kairui Wan, Ke Tang, Linglong Wang, Qin Tian, Mingwei Zheng, Cheng Qian, Limei Liu   +6 more
wiley   +1 more source

Craniometaphyseal and craniodiaphyseal dysplasia, head and neck manifestations and management [PDF]

, 1996
Craniometaphyseal and craniodiaphyseal dysplasia are rare genetic disorders of bone due to modelling errors of long bones and skull bones. These syndromes present with multiple ENT symptomatology from an early age.
Bailey, CM, Dillon, MJ, Richards, A, Brain, C   +3 more
core  

Fibrous dysplasia, Paget's disease of bone, and other uncommon sclerotic bone lesions of the craniofacial bones

, 2020
Imaging studies of the brain, head and neck, sinuses, and dental computed tomography are among the most frequently performed procedures in radiologic departments.
Van de Voorde, Nick, Mortier, Geert R., Vanhoenacker, Filip, Vanhoenacker, Filip M., Nick Van de Voorde, Geert R. Mortier, Filip M. Vanhoenacker   +6 more
core   +1 more source

Management of Refractory and Difficult‐To‐Treat Inflammatory Bowel Disease: An Expert Opinion Review

JCC Plus, Volume 1, Issue 5, September 2026.
This expert opinion offers a practical framework for refractory and difficult‐to‐treat IBD: confirm inflammation objectively, distinguish pharmacologic from structural and functional disease, and then escalate. Across ten clinical questions, the evidence is often limited to case series, and the resulting statements are identified as expert opinion ...
Filiz Akyuz, Oguz Kagan Bakkaloglu, Nalan Gulsen Unal, Ismail Hakki Kalkan, Mehmet Arhan, Ibrahim Hatemi, Taylan Kav, Murat Toruner, Hale Akpinar, Ahmet Tezel, Aykut Ferhat Celik   +10 more
wiley   +1 more source