Results 111 to 120 of about 528 (154)

Muskel-Funktionsanalyse bei Progressiver Diaphysärer Dysplasie (PDD)/Camurati-Engelmann Syndrom (CES) – eine Fallstudie

Osteologie, 2021
Zusammenfassung Hintergrund Das Camurati-Engelmann Syndrom (CES) ist klinisch durch Muskelfunktionsstörungen, Watschelgang und eingeschränkte Mobilität gekennzeichnet, die möglicherweise durch eine diaphysäre Dysplasie getriggert sind.
Christoph Anders, Ben Abendroth, Klaus Abendroth   +2 more
openaire   +1 more source

Camurati Engelmann Syndrome

International Journal of Contemporary Medicine, 2016
Camurati-Engelmann syndrome or progressive diaphyseal dysplasia is a rare autosomal dominant hereditary disorder, characterized by symmetrical progressive sclerosis of long bones cortical diaphysis. Its presentation and progression is extremely variable.
Sheena Gupta, Sanober Wasim, Neerul Pandita, BP Kalra   +3 more
openaire   +1 more source

Zufallsbefund einer progressiven diaphysären Dysplasie (Camurati-Engelmann-Syndrom)

Nuklearmedizin, 1993
ZusammenfassungWir berichten über eine 35jährige Patientin, bei der als Zufallsbefund während einer Phlebographie vor Varizenoperation hyperostotische Veränderungen in Femur- und Tibiadiaphysen im Sinne eines Camurati-Engelmann-Syndroms aufgefallen waren.
U. Büll, R. Bares, B. Grün, C. Altehoefer   +3 more
openaire   +1 more source

[The Camurati-Engelmann syndrome (progressive diaphyseal dysplasia)].

Ceskoslovenska pediatrie, 1992
The presented case-history demonstrates an infant with a rare bone disease with a very serious prognosis. Based on X-ray findings on the skeleton (sclerosis of the diaphyses of long bones, ribs, vertebrae and in particular the base and vault of the skull), the diagnosis of morbus Camurati-Engelmann--progressive diaphyseal dysplasia was established ...
K, Bláhová, J, Horák, I, Marík
openaire   +1 more source

Multiple congenital abnormalities with diaphyseal dysplasia (Camurati—Engelmann's syndrome)

Oral Surgery, Oral Medicine, Oral Pathology, 1969
Abstract A report of a 4 1 2 - year-old child with severe congenital abnormalities consistent with a diagnosis of progeria and associated with Camurati—Engelmann's disease has been presented. Interesting features of the case were the marked sclerotic changes in, and increased density of, the ribs and the mandible.
openaire   +1 more source

[An incidental finding of a progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)].

Nuklearmedizin. Nuclear medicine, 1994
In a 35 year-old female diaphyseal hyperostosis of femur and tibia indicative of a Camurati-Engelmann syndrome (progressive diaphyseal dysplasia) were discovered during routine phlebography. This rare disorder belongs to the group of osteochondrodysplasias and affects primarily the diaphyses of long bones.
C, Altehoefer, B, Grün, R, Bares, U, Büll   +3 more
openaire   +1 more source

[Observations on the Camurati-Engelmann syndrome. Demonstration of changes of the petrous bone using high-resolution computed tomography].

RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 1989
In Camurati-Engelmann disease HR-CT can impressively demonstrate the involvement of the skull base and also correlate well with the clinical symptoms of deafness, vestibular disturbances and facial paralysis. Since conservative treatment with corticosteroids, calcitonin and diphosphonates is hardly successful and compression of the cranial nerves ...
B, Dannenmaier, B, Weber
openaire   +1 more source

[Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].

Deutsche medizinische Wochenschrift (1946), 1981
Radiological changes in the skeleton had been present for 30 years in a now 42-year-old man with diaphyseal dysplasia (Camurati-Engelmann syndrome). Because of threatened blindness by bony narrowing of the optic canal prednisolone was administered over several years.
F, Kuhlencordt, H P, Kruse, K A, Hellner, R, Montz   +3 more
openaire   +1 more source

Beobachtungen zum Camurati-Engelmann-Syndrom

RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren, 1989
B. Dannenmaier, B. Weber
openaire   +1 more source

Evidence for locus heterogeneity in the Camurati–Engelmann (DPD1) Syndrome

Clinical Genetics, 2001
J T, Hecht, S H, Blanton, S, Broussard, A, Scott, C, Rhoades Hall, J M, Milunsky   +5 more
openaire   +2 more sources