Cargando…
Pycnodysostose: à propos d’un cas
Pycnodysostosis is a very rare genetic disease of the bone characterized by osteocondensation associated with dysmorphic syndrome and growth retardation. This study aims to highlight the phenotypic abnormalities, the radiological signs, the therapeutic and evolutionary features of pycnodysostosis in...
Autores principales: | Elyajouri, Abdelhakim, Benyahia, Mohammed, Abilkassem, Rachid, Agadr, Aomar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462148/ https://www.ncbi.nlm.nih.gov/pubmed/31011394 http://dx.doi.org/10.11604/pamj.2018.31.93.8388 |
Ejemplares similares
-
Déficit congénital en facteur V: à propos d’un cas
por: Boujrad, Saloua, et al.
Publicado: (2017) -
Double arc aortique: à propos de deux cas
por: Lemouakni, Sihame, et al.
Publicado: (2017) -
Congenital hyperinsulinsim: case report and review of literature
por: Hasbaoui, Brahim El, et al.
Publicado: (2020) -
Nijmegen breakage syndrome: case report and review of literature
por: Hasbaoui, Brahim El, et al.
Publicado: (2020) -
Pathomimie de l'enfant: à propos d'une observation
por: Abilkassem, Rachid, et al.
Publicado: (2013)