Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mohamed Elabbasy"'
Autor:
Michael P. Schittkowski, Sabine Naxer, Mohamed Elabbasy, Leonie Herholz, Vivian Breitling, Alan Finglas, Jutta Gärtner, Lars Schlotawa
Publikováno v:
Children, Vol 10, Iss 3, p 595 (2023)
Multiple sulfatase deficiency (MSD) is an extremely rare autosomal recessively inherited disease with a prevalence of 1:500.000 caused by mutations on the sulfatase-modifying-Factor 1 gene (SUMF1). MSD is most specifically characterised by a combinat
Externí odkaz:
https://doaj.org/article/37a4e7b9d78944429ab4ced7f6e2610d
Autor:
Michael P. Schittkowski, Stefanie Martius, Mohamed Elabbasy, Steffi Knappe, Rudolf F. Guthoff
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 239:64-72
Zusammenfassung Einleitung Ein kongenitaler Mikrophthalmus kann entweder isoliert auftreten (einfacher Mikrophthalmus) oder mit weiteren okulären Fehlbildungen, wie einer Sklerokornea oder einer Katarakt, assoziiert sein (komplexer Mikrophthalmus).
Publikováno v:
Strabismus. 30(4)
To study the secondary management of strabismus due to third nerve palsy using bovine pericardium (Tutopatch®) when previous conventional surgical therapy had failed. Review of our clinic records of selected patients with third nerve palsy, in whom
Autor:
Michael P, Schittkowski, Stefanie, Martius, Mohamed, Elabbasy, Steffi, Knappe, Rudolf F, Guthoff
Publikováno v:
Klinische Monatsblatter fur Augenheilkunde. 239(1)
Congenital microphthalmos can either occur alone (simple microphthalmos) or be associated with other ocular malformations, such as sclerocornea or cataract (complex microphthalmos). As this is a rare condition, there are no uniform recommendations fo