A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

MK Prasad, V Geoffroy, S Vicaire, B Jost… - Journal of medical …, 2016 - jmg.bmj.com
Background Orodental diseases include several clinically and genetically heterogeneous
disorders that can present in isolation or as part of a genetic syndrome. Due to the vast …

Enamel–renal syndrome with congenital heart defects and asthma: a rare association in a Moroccan child

S Laouina, AB Zupan - Clinical dysmorphology, 2017 - journals.lww.com
Enamel–renal syndrome (ERS, OMIM 204690) is an autosomal recessive disorder
characterized by severe enamel hypoplasia on the primary and secondary dentition, pulp …

[HTML][HTML] A rare association-amelogenesis imperfecta, platispondyly and bicytopenia: a case report

S Laouina, S Chafai El Alaoui, R Amezian… - Journal of Medical Case …, 2015 - Springer
Introduction Amelogenesis imperfecta is an inherited disease characterized by generalized
structural abnormalities of the enamel on all teeth, including both primary and permanent …

[PDF][PDF] Etude clinique et moléculaire des amélogenèses imparfaites chez des familles marocaines

S Laouina - 2017 - toubkal.imist.ma
Les maladies rares sont définies par leur faible prévalence. Selon L'Union européenne
(UE), une maladie rare est une maladie qui touche moins d'une personne sur 2000. En …

[CITATION][C] AMELOGENESE IMPARFAITE HEREDITAIRE: ETUDE CLINIQUE HISTOLOGIQUE ET/OU GENETIQUE

L SAMIR - 2016 - otrohati.imist.ma
AMELOGENESE IMPARFAITE HEREDITAIRE : ETUDE CLINIQUE HISTOLOGIQUE ET/OU
GENETIQUE Catalogue des thèses Marocaine en cour AMELOGENESE IMPARFAITE …