Le nanisme thanatophore est une ostéochondrodysplasie due à une mutation du gène FGFR3 (fibroblast growth factor receptor 3) localisé sur le bras court du Chromosome 4. Il est caractérisée par une macrocranie, un raccourcissement des membres, un thorax étroit et un abdomen proéminant reconnu, en anténatal à l’échographie et à la radiographie du contenu utérin. Ce diagnostic peut également être évoqué en post natal par l’examen clinique et la radiographie du nouveau-né qui met en évidence les mêmes éléments. C’est une malformation létale rare. Le dépistage anténatal précoce permet de proposer une interruption thérapeutique de la grossesse à la gestante dans le but de lui éviter tout traumatisme psychologique et obstétrical.Nous rapportons de...
The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dyspla...
Introduction. Obstetric ultrasonography is routinely used to screen for fetal anomalies. Thanatophor...
[[abstract]]Abstract Objective We present perinatal imaging findings and molecular genetic analysis...
Le nanisme thanatophore est une osteochondrodysplasie rare classee en deux types I et II. Elle est d...
Thanatophoric dysplasia (TD) was reported earlier in the previous publication. It is one of the mos...
Abstract (English) Objective: To report a rare case of thanatophoric skeletal dysplasia type 2 that ...
Thanatophoric dysplasia is the lethal skeletal dysplasia characterized by marked underdevelopment of...
A thanatophoric dysplasia type / case with a FGFR3 p.R248C mutation and survival beyond the neonatal...
Thanatophore dysplasia is a rare lethal bone dysplasia. It is caused bya genetic mutation. There are...
A thanatophoric dysplasia type I case with a FGFR3 p.R248C mutation and survival beyond the neonatal...
Background: Thanatophoric dysplasia (TD) is the most lethal and most severe type of dysplasia. It ha...
Thanatophoric dysplasia (TD), a rare and lethal skeletal dysplasia of neonatal period. Two clinical ...
Thanatophoric dysplasia type 1 is a form of lethal skeletal dysplasia, characterized by axial-append...
Thanatophoric Dysplasia (TD) is a congenital, sporadic and most lethal skeletal dysplasia caused by ...
Thanatophoric dysplasia is a lethal form of skeletal dysplasia seen in neonates. The word ‘thanatoph...
The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dyspla...
Introduction. Obstetric ultrasonography is routinely used to screen for fetal anomalies. Thanatophor...
[[abstract]]Abstract Objective We present perinatal imaging findings and molecular genetic analysis...
Le nanisme thanatophore est une osteochondrodysplasie rare classee en deux types I et II. Elle est d...
Thanatophoric dysplasia (TD) was reported earlier in the previous publication. It is one of the mos...
Abstract (English) Objective: To report a rare case of thanatophoric skeletal dysplasia type 2 that ...
Thanatophoric dysplasia is the lethal skeletal dysplasia characterized by marked underdevelopment of...
A thanatophoric dysplasia type / case with a FGFR3 p.R248C mutation and survival beyond the neonatal...
Thanatophore dysplasia is a rare lethal bone dysplasia. It is caused bya genetic mutation. There are...
A thanatophoric dysplasia type I case with a FGFR3 p.R248C mutation and survival beyond the neonatal...
Background: Thanatophoric dysplasia (TD) is the most lethal and most severe type of dysplasia. It ha...
Thanatophoric dysplasia (TD), a rare and lethal skeletal dysplasia of neonatal period. Two clinical ...
Thanatophoric dysplasia type 1 is a form of lethal skeletal dysplasia, characterized by axial-append...
Thanatophoric Dysplasia (TD) is a congenital, sporadic and most lethal skeletal dysplasia caused by ...
Thanatophoric dysplasia is a lethal form of skeletal dysplasia seen in neonates. The word ‘thanatoph...
The rare form of skeletal dysplasia is thanatophoric dysplasia. The meaning for thanatophoric dyspla...
Introduction. Obstetric ultrasonography is routinely used to screen for fetal anomalies. Thanatophor...
[[abstract]]Abstract Objective We present perinatal imaging findings and molecular genetic analysis...