Results 51 to 60 of about 903 (178)
Veterinary Radiology &Ultrasound, Volume 66, Issue 1, January 2025.Abstract Laying hens are increasingly being kept in backyard flocks and considered family pets; however, diagnostic imaging characteristics of bone for clinically normal backyard hens are currently limited. This prospective, descriptive study was to describe radiographic, computed tomographic, and histologic characteristics of bone for a group of ...
Jeryl Jones +3 more
wiley +1 more source
A novel LEMD3 mutation common to patients with osteopoikilosis with and without melorheostosis
, 2007 Recent studies have reported loss of function mutations in the LEMD3 gene, encoding an inner nuclear membrane protein that influences Smad signaling, as a cause of osteopoikilosis, Buschke-Ollendorff syndrome, and melorheostosis. We investigated LEMD3 in
Peach, Chris A. +13 more
core +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
Epidemiological, clinical and radiological aspects of osteopoikilosis
, 1992 Osteopoikilosis is a rare condition showing characteristic sclerotic lesions on radiographic examination, which are diagnostic for the trait. We report four patients presenting with various complaints and 49 members of their families who later were ...
S Akalin +5 more
core +1 more source
Osteomesopyknosis associated with a novel ALOX5 variant that impacts the RANKL pathway
Molecular Genetics &Genomic Medicine, Volume 12, Issue 5, May 2024.Osteomesopyknosis is a rare bone sclerosing disorder of unelucidated pathophysiology with a presumably autosomal dominant transmission. However, the causal genes are unknown. Here we report a new case of osteomesopyknosis associated with a missense ALOX5 variant predicted to induce protein misfolding and proteasomal degradation.
Jose L. Fernandez‐Luna +10 more
wiley +1 more source
De Quervain's syndrome associated with osteopoikilosis: a case report and review of the literature
, 2009 Osteopoikilosis is a rare, usually asymptomatic, autosomal-dominant bone disorder, which is generally diagnosed incidentally on X-ray. De Quervain's syndrome is a disorder characterized by pain on the radial (thumb) side of the wrist, impairment of thumb
Akarirmak, Ulku +7 more
core +1 more source
Disorders associated with osteopoikilosis - 5 different lesions in a family
, 2003 Although osteopoikilosis is generally considered an accidental finding, several developmental dysplasias coexisting with this disorder have been reported. However, all authors have mentioned only one coexisting finding, and most of them are case reports.
Kiter, E +3 more
core +1 more source
Osteopoikilosis: A case report with review of literature
Journal of Orthopedics, Traumatology and Rehabilitation, 2013 Osteopoikilosis is a rare hereditary condition present as an autosomal dominant trait in families, but can also present as sporadic cases. It is an asymptomatic condition; incidental radiological finding play an important role in its diagnosis. These are
Daya Krishna, Subhash Chand
doaj +1 more source
Elastoma: clinical and histopathological aspects of a rare disease [PDF]
Anais Brasileiros de Dermatologia, 2016 Elastoma is a connective tissue nevus characterized by changes in elastic fibers. It can be congenital or acquired, and is usually diagnosed before puberty. Associated with osteopoikilosis, it is known as Buschke-Ollendorff syndrome.
Marina Gagheggi Maciel +5 more
doaj +2 more sources
Osteopoikilosis: A case with osteopenia
, 2009 Osteopoikilosis is a benign osteosclerotic dysplasia of unknown origin, which is an inherited autosomal disorder. It is usually asymptomatic and may only be recognized on radiological examination.
ZİNNUROĞLU, MURAT +2 more
core +1 more source