Results 31 to 40 of about 2,247 (190)

Longitudinal Observation of Changes in the Ankle Alignment and Tibiofibular Relationships in Hereditary Multiple Exostoses. [PDF]

open access: yesDiagnostics (Basel), 2020
The longitudinal changes in the tibiofibular relationship as the ankle valgus deformity progresses in patients with hereditary multiple exostoses (HME) are not well-known.
Lee JH   +5 more
europepmc   +4 more sources

A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate. [PDF]

open access: yesGenet Mol Biol, 2021
Hereditary multiple exostoses (HME) is a rare skeletal disorder characterized by the formation of multiple benign cartilage-capped tumors, usually in the metaphyseal region of the long bones.
Xian C   +12 more
europepmc   +2 more sources

Spinal Exostosis in a Boy with Multiple Hereditary Exostoses

open access: yesCase Reports in Orthopedics, 2013
We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal.
Ali Al Kaissi   +3 more
doaj   +1 more source

Osteochondroma of rib cage in a case of HME: A rare presentation

open access: yesJournal of Orthopaedic Reports, 2023
Background: Osteochondroma is the most common benign bone tumor. This aberrant developmental lesion of the bone in the rib is rare and forms part of multiple diaphyseal aclasia in some cases.
Saroj prasad Sah   +5 more
doaj   +1 more source

Osteochondroma of Upper Dorsal Spine Causing Spastic Paraparesis in Hereditary Multiple Exostosis: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Osteochondroma of the spine is rare. It may present in solitary or multiple form (hereditary multiple exostoses). Herein, we report a case of an 18-year-old male who was diagnosed with thoracic osteochondroma, originating from the D4 vertebra with ...
Gaurav Kumar Upadhyaya   +4 more
doaj   +1 more source

Reconstruction of the Hip in Multiple Hereditary Exostoses

open access: yesChildren, 2021
The hip joint involvement in multiple hereditary exostoses (MHE) occurs in 30–90%, causing pain and limitation of motion by femoroacetabular impingement, coxa valga, acetabular dysplasia, hip joint subluxation, and osteoarthritis.
Dong Hoon Lee, Dror Paley
doaj   +1 more source

Arthroscopic Anterior Cruciate Ligament Reconstruction in a 17-Year-Old Female Athlete with Multiple Hereditary Exostoses Using a Peroneus Longus Autograft: A Rare Case Report

open access: yesJournal of Orthopaedic Case Reports
Introduction: Hereditary multiple exostoses, also known as multiple osteochondromas, is a rare genetic disorder marked by the formation of osteocartilaginous outgrowths predominantly near the metaphysis of long bones.
Sanjay Singh Chauhan   +2 more
doaj   +1 more source

Tooth row allometry in domestic rabbits and nondomestic lagomorphs: Evidence for a decoupling of body and tooth row size changes in evolutionary time

open access: yesThe Anatomical Record, EarlyView.
Domestic rabbits of different body sizes differ disproportionately in the length of their tooth row or the length of their diastema. Abstract In various domestic mammals, smaller breeds tend to have proportionally larger teeth, whereas this is not a universal trend across mammals.
Ursina L. Fasciati   +3 more
wiley   +1 more source

Acetabular dysplasia associated with hereditary multiple exostoses

open access: yes, 2000
Hereditary multiple exostoses is an autosomal dominant disorder characterised by multiple osteochondromata, most commonly affecting the forearm, knee and ankle. Osteochondromata of the proximal femur have been reported to occur in 30% to 90% of affected
E. A. Loveless, N. A. Felix, J. M. Mazur
core   +1 more source

Congenital multiple exostoses with congenital heart disease

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Multiple exostoses are a rare disorder. It is estimated to occur in 1; 50,000 pregnancies. It presents within the first decade of life and it has an autosomal mode of inheritance; though it has been associated with a spontaneous mutation in 10% of cases.
Ibrahim Aliyu, Teslim O Lawal
doaj   +1 more source

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