Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mariam Mngoya"'
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Pfieffer syndrome is among the syndromes seen in the recognized variant of the FGFR2 gene. There are several conditions related to this variant and a very closely related condition is Crouzon syndrome. This case is important to re
Externí odkaz:
https://doaj.org/article/bbed7188a218409b981643e1d95d969e
Autor:
Insiyah A. Amiji, Ummulkheir H. Mohamed, Adelina G. Rutashobya, Mariam Mngoya, Nicole Schoenmann, Helga E. Naburi, Karim P. Manji
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-6 (2019)
Abstract Introduction De Morsier syndrome, or septo-optic dysplasia, is a rare, heterogeneous, complex condition with a highly variable phenotype. It is characterized by optic nerve hypoplasia, pituitary gland hypoplasia, and midline brain abnormalit
Externí odkaz:
https://doaj.org/article/d47b0a0b96274603a4af1a1437995d91
Autor:
Manji, Karim P.1 (AUTHOR) kpmanji@gmail.com, Massomo, Mariam Mngoya2 (AUTHOR), Akyoo, Edna Samson2 (AUTHOR), Luvinga, McLean Abisai2 (AUTHOR)
Publikováno v:
Journal of Medical Case Reports. 11/1/2022, Vol. 16 Issue 1, p1-5. 5p.
Publikováno v:
BMJ Case Reports; Jun2023, Vol. 16 Issue 6, p1-3, 3p