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.43748-5
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...
PubMed ID: 8826753We report the imaging findings in a 3 year old girl with a mild form of holoprosen...
We report on a child with midline facial defects with hypertelorism (MFDH), median cleft lip, spheno...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
We studied the neuroimaging and neurophysiological aspects of 17 patients with midline facial defect...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Developmental midline abnormalities involving facial, optic, cranial, and cerebral structures are co...
Objective: Twenty-four patients were evaluated to better characterize neurological and neuroradiolog...
Objectives: We studied the neuroimaging and neurophysiological aspects of 17 patients with midline f...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
Clinical picture and skull radiographs of a patient having a developmental field defect, probably oc...
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...
PubMed ID: 8826753We report the imaging findings in a 3 year old girl with a mild form of holoprosen...
We report on a child with midline facial defects with hypertelorism (MFDH), median cleft lip, spheno...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
We studied the neuroimaging and neurophysiological aspects of 17 patients with midline facial defect...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
Developmental midline abnormalities involving facial, optic, cranial, and cerebral structures are co...
Objective: Twenty-four patients were evaluated to better characterize neurological and neuroradiolog...
Objectives: We studied the neuroimaging and neurophysiological aspects of 17 patients with midline f...
In order to contribute to clinical delineation of midline facial defects with hypertelorism (MFDH) a...
The aim of this study were to describe and to compare structural central nervous system (CNS) anomal...
Clinical picture and skull radiographs of a patient having a developmental field defect, probably oc...
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...
PubMed ID: 8826753We report the imaging findings in a 3 year old girl with a mild form of holoprosen...