Cargando…

A Constellation of Orthopaedic Deformities in Connection with Cartilage Oligomeric Matrix Protein Mutation

BACKGROUND: Trendelenburg's gait can be observed in Legg-Calvé-Perthes disease, antalgic gait observed in osteoarthropathy and waddling gait is usually seen in genu varum and circumduction gait in patients with genu valgum. Disabling pain was a prime manifestation in slipped capital femoral epi...

Descripción completa

Detalles Bibliográficos
Autores principales:	Al Kaissi, Ali, Ghachem, Maher Ben, Kenis, Vladimir, Melchenko, Eugene, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7759081/ https://www.ncbi.nlm.nih.gov/pubmed/32952136 http://dx.doi.org/10.4103/ajps.AJPS_90_17

Ejemplares similares

The constellation of skeletal deformities in a family with mixed types of mucopolysaccharidoses: Case report
por: Kaissi, Ali Al, et al.
Publicado: (2016)

Corrections of diverse forms of lower limb deformities in patients with mucopolysaccharidosis type IVA (Morquio syndrome)
por: Al Kaissi, Ali, et al.
Publicado: (2016)

The Diversity of the Clinical Phenotypes in Patients With Fibrodysplasia Ossificans Progressiva
por: Al Kaissi, Ali, et al.
Publicado: (2016)

Massive Axial and Appendicular Skeletal Deformities in Connection with Gorham-Stout Syndrome
por: Al Kaissi, Ali, et al.
Publicado: (2019)

Spinal and extraspinal deformities in a patient with dysspondyloenchondromatosis
por: Kenis, Vladimir, et al.
Publicado: (2013)

How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports
por: Al Kaissi, Ali, et al.
Publicado: (2017)

Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan
por: Al Kaissi, Ali, et al.
Publicado: (2019)

Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article
por: Kaissi, Ali Al, et al.
Publicado: (2020)

Can Multiple Hereditary Exostoses Overlap With Mesomelic Dysplasia?
por: Al Kaissi, Ali, et al.
Publicado: (2016)

Muscle Weakness: A Misleading Presentation in Children With Distinctive Syndromic Entities (Clinical Case Reports)
por: Al Kaissi, Ali, et al.
Publicado: (2017)

Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports
por: Al Kaissi, Ali, et al.
Publicado: (2017)

Turning the backbone into an ankylosed concrete-like structure: Case report
por: Kaissi, Ali Al, et al.
Publicado: (2018)

The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational study
por: Al Kaissi, Ali, et al.
Publicado: (2019)

Spine malformation complex in 3 diverse syndromic entities: Case reports
por: Kaissi, Ali Al, et al.
Publicado: (2016)

Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen–Goldberg syndrome: a report on a family over 4 generations: Case report
por: Al Kaissi, Ali, et al.
Publicado: (2017)

Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
por: Al Kaissi, Ali, et al.
Publicado: (2023)

Progressive Deformity of the Lower Limbs in a Patient with KID (Keratitis-Ichthyosis-Deafness) Syndrome
por: Kozhevnikov, Oleg, et al.
Publicado: (2020)

Management of progressive genu varum in a patient with Dyggve-Melchior-Clausen syndrome
por: Kenis, Vladimir, et al.
Publicado: (2011)

Correction of the axial and appendicular deformities in a patient with Silver-Russel syndrome
por: Al Kaissi, Ali, et al.
Publicado: (2015)

Treatment of Varus Deformities of the Lower Limbs in Patients with Achondroplasia and Hypochondroplasia
por: Kaissi, Ali Al, et al.
Publicado: (2013)

Varus deformity of the left lower extremity causing degenerative lesion of the posterior horn of the left medial meniscus in a patient with Paget’s disease of bone
por: Al Kaissi, Ali, et al.
Publicado: (2014)

Agenesis of the Corpus Callosum and Skeletal Deformities in Two Unrelated Patients: Analysis via MRI and Radiography
por: Al Kaissi, Ali, et al.
Publicado: (2014)

Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives
por: Al Kaissi, Ali, et al.
Publicado: (2023)

The Tomographic Study and the Phenotype of Wormian Bones
por: Al Kaissi, Ali, et al.
Publicado: (2023)

Significant ophthalmoarthropathy associated with ectodermal dysplasia in a child with Marshall-Stickler overlap: a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

The management of knee dislocation in a child with Larsen syndrome
por: Kaissi, Ali Al, et al.
Publicado: (2011)

Cervico-thoracic kyphosis in a girl with Pierre Robin sequence
por: Al Kaissi, Ali, et al.
Publicado: (2011)

Swellings over the Limbs as the Earliest Feature in a Patient with Osteogenesis Imperfecta Type V
por: Al Kaissi, Ali, et al.
Publicado: (2014)

Spinal Exostosis in a Boy with Multiple Hereditary Exostoses
por: Al Kaissi, Ali, et al.
Publicado: (2013)

Bilateral and Symmetrical Anteromedial Bowing of the Lower Limbs in a Patient with Neurofibromatosis Type-I
por: Al Kaissi, Ali, et al.
Publicado: (2015)

Distinctive Skeletal Abnormalities With No Microdeletions or Microduplications on Array-CGH in a Boy With Mohr Syndrome (Oro-Facial-Digital Type II)
por: Kaissi, Ali Al, et al.
Publicado: (2015)

Broad Spectrum of Skeletal Malformation Complex in Patients with Cleidocranial Dysplasia Syndrome: Radiographic and Tomographic Study
por: Al Kaissi, Ali, et al.
Publicado: (2013)

Radiographic and Tomographic Analysis in Patients with Stickler Syndrome Type I
por: Al Kaissi, Ali, et al.
Publicado: (2013)

Neonatal Death Dwarfism in a Girl with Distinctive Bone Dysplasia Compatible with Grebe Chondrodysplasia: Analysis by CT Scan-based Phenotype
por: Al Kaissi, Ali, et al.
Publicado: (2014)

Progressive non-infectious anterior vertebral fusion, split cord malformation and situs inversus visceralis
por: Al Kaissi, Ali, et al.
Publicado: (2006)

Ischiopubic and odontoid synchondrosis in a boy with progressive pseudorheumatoid chondrodysplasia
por: Al Kaissi, Ali, et al.
Publicado: (2007)

Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities
por: Al Kaissi, Ali, et al.
Publicado: (2022)

Achondroplasia manifesting as enchondromatosis and ossification of the spinal ligaments: a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Extended phenotypes in a boy and his mother with oto-palato-digital-syndrome type II
por: Kaissi, Ali Al, et al.
Publicado: (2015)

Torticollis in Connection with Spine Phenotype
por: Al Kaissi, Ali, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_1jbqi7k61s9taopc5i8492lnfb