Cargando…

Arthrogryposis multiplex congenital in a child manifesting phenotypic features resembling dysosteosclerosis/osteosclerosis malformation complex; 3DCT scan analysis of the skull base

INTRODUCTION: A boy presented with arthrogryposis multiplex congenita (AMC) associated with severe central nervous system dysfunction. The clinical history and the distinctive radiographic/tomographic features were consistent but not completely diagnostic for dysosteosclerosis. CASE PRESENTATION: A...

Descripción completa

Detalles Bibliográficos
Autores principales:	Al Kaissi, Ali, Kalchhauser, Georg, Grill, Franz, Klaushofer, Klaus
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2008
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526066/ https://www.ncbi.nlm.nih.gov/pubmed/18651947 http://dx.doi.org/10.1186/1757-1626-1-56

Ejemplares similares

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

Professional awareness is needed to distinguish between child physical abuse from other disorders that can mimic signs of abuse (Skull base sclerosis in infant manifesting features of infantile cortical hyperostosis): a case report and review of the literature
por: Al Kaissi, Ali, et al.
Publicado: (2009)

A novel malformation complex of bilateral and symmetric preaxial radial ray-thumb aplasia and lower limb defects with minimal facial dysmorphic features: a case report and literature review
por: Al Kaissi, Ali, et al.
Publicado: (2008)

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

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

A patient with Melorheostosis manifesting with features similar to tricho-dento-osseous syndrome: a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome
por: Kaissi, Ali Al, et al.
Publicado: (2007)

Arthrogryposis multiplex congenita—an update
por: Møller-Madsen, Bjarne
Publicado: (2015)

Localised Osteosclerosis
Publicado: (1931)

Ball and socket ankle joint in connection with bilateral tarsal synostosis in a boy with congenital absence of the portal vain: a novel malformation complex
por: Zandieh, Shahin, et al.
Publicado: (2008)

Arthrogryposis multiplex congenita: An anesthetic challenge
por: Pujari, Vinayak Seenappa, et al.
Publicado: (2012)

Brown Tumour in the Mandible and Skull Osteosclerosis Associated with Primary Hyperparathyroidism – A Case Report
por: Popovik-Monevska, Danica, et al.
Publicado: (2018)

Intramedullary Osteosclerosis of the Tibia: A Rare Cause of Osteosclerosis to Keep an Eye On
por: Al-Taie, Alaa, et al.
Publicado: (2023)

Progressive joint limitations as the first alarming signs in a boy with short – limbed dwarfism: A case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Outward bulging of the right parietal bone in connection with fibrous dysplasia in an infant: a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Osteochondritis dissecans and Osgood Schlatter disease in a family with Stickler syndrome
por: Al Kaissi, Ali, et al.
Publicado: (2009)

Caudal regression syndrome and popliteal webbing in connection with maternal diabetes mellitus: a case report and literature review
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Progressive acetabular dysplasia in a boy with mucopolysaccharoidosis type IV A (Morquio syndrome): a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

Occipito-Vertebral Dissociation in Connection with Extensive Cervical Spine Malsegmentation in a Boy with Möbius Syndrome
por: Kaissi, Ali Al, et al.
Publicado: (2009)

Severe Skew Foot Deformity in a Patient With Freeman-Sheldon Syndrome
por: Kaissi, Ali Al, et al.
Publicado: (2011)

Tomographic assessment of the spine in children with spondylocostal dysotosis syndrome
por: Kaissi, Ali Al, et al.
Publicado: (2010)

Synophyrs, curly eyelashes and Ptyrigium colli in a girl with Desbuquois dysplasia: a case report and review of the literature
por: Al Kaissi, Ali, et al.
Publicado: (2009)

Distinctive Tomographic Abnormalities of the Craniocervical Region in a Patient with Osteogensis Imperfecta Type IV B
por: Kaissi, Ali Al, et al.
Publicado: (2010)

Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity
por: Turan, Serap, et al.
Publicado: (2022)

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

Diagnosing Arthrogryposis Multiplex Congenita: A Review
por: Kalampokas, Emmanouil, et al.
Publicado: (2012)

Walking ability in patients with arthrogryposis multiplex congenita
por: Eamsobhana, Perajit, et al.
Publicado: (2014)

A Case Report of Dysosteosclerosis Observed from the Prenatal Period
por: Kobayashi, Kisho, et al.
Publicado: (2010)

Femoral-tibial-synostosis in a child with Roberts syndrome (Pseudothalidomide): a case report
por: Al Kaissi, Ali, et al.
Publicado: (2008)

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)

Advanced ossification of the carpal bones, and monkey wrench appearance of the femora, features suggestive of a propable mild form of desbeqious dysplasia: a case report and review of the literature
por: Al Kaissi, Ali, et al.
Publicado: (2009)

Acroform type of enchondromatosis associated with severe vertebral involvement and facial dysmorphism in a boy with a new variant of enchondromatosis type I1 of Spranger: case report and a review of the literature
por: Kaissi, Ali Al, et al.
Publicado: (2008)

Significant traumatic atrophy of the spinal cord in connection with severe cervical vertebral body hypoplasia in a boy with Larsen syndrome: a case report and review of the literature
por: Al Kaissi, Ali, et al.
Publicado: (2009)

Mid-diaphyseal Endosteal Thickening With Subsequent Medullary Narrowing in a Patient With Hallermann-Streiff 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)

Acute Myelocythæmia Associated with Osteosclerosis
por: Goodall, Alexander
Publicado: (1912)

Cannot write session to /tmp/vufind_sessions/sess_odlaj8oc13lo1vnsqdf52st3u5