Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tamer Ahmed EL-Sobky"'
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 48, Iss 1, Pp 237-243 (2017)
Malignant infantile autosomal recessive osteopetrosis (ARO) is rare hereditable skeletal dysplasia characterized by a generalized osteosclerosis. ARO usually runs a fatal course in early childhood if untreated. Serious complications can arise from bo
Externí odkaz:
https://doaj.org/article/f90beb6f0afc445fade4fd8e03892323
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 48, Iss 1, Pp 245-250 (2017)
Pseudoachondroplasia is a rare osteochondrodysplasia characterized by disproportionate short stature and limb deformity. Diagnostic accuracy is based on a detailed evaluation of the radioclinical features. We report a boy with pseudoachondroplasia. W
Externí odkaz:
https://doaj.org/article/66600805815144f39a691417b1760054
Publikováno v:
The Egyptian Journal of Radiology and Nuclear Medicine, Vol 47, Iss 4, Pp 1613-1616 (2016)
Primary hyperparathyroidism (PHPT) is rare in children and adolescents, but has greater morbidity in this age group. Most of these patients show predominantly skeletal pathology and to a lesser extent renal involvement. Osteopenia, osteoporosis and s
Externí odkaz:
https://doaj.org/article/a58b2732e91a44c8b51e159d0f906a6b
Autor:
Karim Elhusseiny, Tamer Ahmed El-Sobky
Publikováno v:
Oman Medical Journal, Vol 33, Iss 5, Pp 444-446 (2018)
A four-year-old otherwise healthy girl presented to our outpatient clinic complaining of left elbow pain and swelling. The child’s parents reported an indoor trauma the previous day. On clinical examination, the left elbow and forearm exhibited dif
Externí odkaz:
https://doaj.org/article/a275568903d34e8abcd0c5792fbc1ef0
Publikováno v:
Bone Reports, Vol 4, Iss C, Pp 11-16 (2016)
Background: Osteopetrosis is a rare hereditary metabolic bone disorder characterized by generalized skeletal sclerosis caused by a defect in bone resorption and remodelling. Infantile autosomal recessive osteopetrosis is one of three subtypes of oste
Externí odkaz:
https://doaj.org/article/ba87db9d05504accbace85e4ac9602d6
Publikováno v:
Bone Reports, Vol 3, Iss C, Pp 104-108 (2015)
Background: Proteus syndrome is a rare developmental disorder of unknown aetiology. It is a disorder characterized by postnatal overgrowth affecting multiple tissues. Proteus syndrome is most frequently manifested in skeletal changes. As manifestatio
Externí odkaz:
https://doaj.org/article/ea848ccb8cc141fc816768d545646118
Publikováno v:
Case Reports in Pathology, Vol 2015 (2015)
Fungi are unusual causes of pedal osteomyelitis in children and adolescents. Eumycetoma is a chronic cutaneous and subcutaneous infection caused by various genera of fungi. A provisional diagnosis of foot mycetoma is made after clinical assessment. R
Externí odkaz:
https://doaj.org/article/7e252b3ae4a8427a988ccdfa7334c34e