Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
AJNR Am J Neuroradiol ; 39(2): 380-384, 2018 02.
Article in English | MEDLINE | ID: mdl-29170271

ABSTRACT

Thanatophoric dysplasia, achondroplasia, and hypochondroplasia belong to the fibroblast growth factor receptor 3 (FGFR3) group of genetic skeletal disorders. Temporal lobe abnormalities have been documented in thanatophoric dysplasia and hypochondroplasia, and in 1 case of achondroplasia. We retrospectively identified 13 children with achondroplasia who underwent MR imaging of the brain between 2002 and 2015. All children demonstrated a deep transverse temporal sulcus on MR imaging. Further common neuroimaging findings were incomplete hippocampal rotation (12 children), oversulcation of the mesial temporal lobe (11 children), loss of gray-white matter differentiation of the mesial temporal lobe (5 children), and a triangular shape of the temporal horn (6 children). These appearances are very similar to those described in hypochondroplasia, strengthening the association of temporal lobe malformations in FGFR3-associated skeletal dysplasias.


Subject(s)
Achondroplasia/pathology , Temporal Lobe/abnormalities , Achondroplasia/diagnostic imaging , Achondroplasia/genetics , Child , Female , Humans , Magnetic Resonance Imaging , Male , Mutation , Neuroimaging , Phenotype , Receptor, Fibroblast Growth Factor, Type 3/genetics , Retrospective Studies , Temporal Lobe/diagnostic imaging
SELECTION OF CITATIONS
SEARCH DETAIL
...