We report on a child with midline facial defects with hypertelorism (MFDH), median cleft lip, sphenoidal ventriculocele, partial agenesis of the corpus callosum, and low-grade astrocytoma in the cervicomedullary junction. This combination of findings has not been reported previously. Although this association might be casual, it demonstrates a relationship between disorders of frontonasal process and posterior fossae. It also suggests that individuals with MFDH might require a prospective follow-up with central nervous system magnetic resonance imaging.43674875
Hemimegalencephaly (HME) is a rare congenital malformation of the brain, grossly characterized by en...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus ca...
We report on a child with midline facial defects with hypertelorism (MFDH), median cleft lip, spheno...
We studied the neuroimaging and neurophysiological aspects of 17 patients with midline facial defect...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Objectives: We studied the neuroimaging and neurophysiological aspects of 17 patients with midline f...
Objective: Twenty-four patients were evaluated to better characterize neurological and neuroradiolog...
Developmental midline abnormalities involving facial, optic, cranial, and cerebral structures are co...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Clinical picture and skull radiographs of a patient having a developmental field defect, probably oc...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus ca...
SUMMARY Basal encephaloceles are often associated with other midline anomalies such as hyper-teloris...
Hemimegalencephaly (HME) is a rare congenital malformation of the brain, grossly characterized by en...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus ca...
We report on a child with midline facial defects with hypertelorism (MFDH), median cleft lip, spheno...
We studied the neuroimaging and neurophysiological aspects of 17 patients with midline facial defect...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Objectives: We studied the neuroimaging and neurophysiological aspects of 17 patients with midline f...
Objective: Twenty-four patients were evaluated to better characterize neurological and neuroradiolog...
Developmental midline abnormalities involving facial, optic, cranial, and cerebral structures are co...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Clinical picture and skull radiographs of a patient having a developmental field defect, probably oc...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus ca...
SUMMARY Basal encephaloceles are often associated with other midline anomalies such as hyper-teloris...
Hemimegalencephaly (HME) is a rare congenital malformation of the brain, grossly characterized by en...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
We describe a female patient with a midline syndrome. The patient presents agenesis of the corpus ca...