Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformational changes resulting from decreased or absent fetal movement, and include arthrogryposis, and craniofacial and central nervous system anomalies. We report an autopsy case of a 36-6/7week female neonate with a normal female karyotype and chromosome microarray demonstrating findings consistent with FADS. We provide a detailed examination of the severe and complex central nervous system abnormalities, including marked pontocerebellar hypoplasia and cortical and cerebellar migration and gyration defects. This case represents a rare detailed examination of the central nervous system of a patient with FADS
The fetal brain disruption sequence (FBDS), a rare cause of extreme microcephaly, is described in a ...
Rat fetuses were paralyzed by daily transuterine injections of curare from day 18 of gestation until...
[[abstract]]Fetal akinesia deformation sequence is a clinically and genetically heterogeneous disord...
Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformat...
Fetal Akinesia Deformation Sequence (FADS) is a condition characterised by decreased fetal movement ...
International audienceTubulinopathies are increasingly emerging major causes underlying complex cere...
Fakinesia deformation sequence (FADS) represents a group of disorders resulting from absent or dimin...
Background: Fetal Akinesia Deformation Sequence (FADS) is a rare, in most cases autosomal recessive,...
In this paper we report a case of early onset fetal akinesia, with unusual pathological findings. T...
International audienceFoetal akinesia deformation sequence syndrome (FADS) is a heterogenous disorde...
The development of the human cerebral cortex is a complex and precisely programmed process by which ...
Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardat...
BACKGROUND: Fetal akinesia deformation sequence syndrome (FADS) is a heterogeneous disorder characte...
AbstractFetal akinesia deformation sequence is a clinically and genetically heterogeneous disorder c...
We report on the detection of discordant inclusions in the brain of a 25-week female fetus with a ve...
The fetal brain disruption sequence (FBDS), a rare cause of extreme microcephaly, is described in a ...
Rat fetuses were paralyzed by daily transuterine injections of curare from day 18 of gestation until...
[[abstract]]Fetal akinesia deformation sequence is a clinically and genetically heterogeneous disord...
Fetal akinesia deformation sequence (FADS), or Pena-Shokeir phenotype is a constellation of deformat...
Fetal Akinesia Deformation Sequence (FADS) is a condition characterised by decreased fetal movement ...
International audienceTubulinopathies are increasingly emerging major causes underlying complex cere...
Fakinesia deformation sequence (FADS) represents a group of disorders resulting from absent or dimin...
Background: Fetal Akinesia Deformation Sequence (FADS) is a rare, in most cases autosomal recessive,...
In this paper we report a case of early onset fetal akinesia, with unusual pathological findings. T...
International audienceFoetal akinesia deformation sequence syndrome (FADS) is a heterogenous disorde...
The development of the human cerebral cortex is a complex and precisely programmed process by which ...
Seckel syndrome is a rare autosomal recessive disorder characterized by intrauterine growth retardat...
BACKGROUND: Fetal akinesia deformation sequence syndrome (FADS) is a heterogeneous disorder characte...
AbstractFetal akinesia deformation sequence is a clinically and genetically heterogeneous disorder c...
We report on the detection of discordant inclusions in the brain of a 25-week female fetus with a ve...
The fetal brain disruption sequence (FBDS), a rare cause of extreme microcephaly, is described in a ...
Rat fetuses were paralyzed by daily transuterine injections of curare from day 18 of gestation until...
[[abstract]]Fetal akinesia deformation sequence is a clinically and genetically heterogeneous disord...