Sporadic fetal brain disruption sequence
Sporadic fetal brain disruption sequence is a rare non-syndromic central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD) overlapping sutures keel-like occipital bone prominence scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly cortical tissue deficit and hydranencephaly.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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Sporadic fetal brain disruption sequence?
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Advocacy Organizations
COMBINEDBrain Inc
COMBINEDBrain is a consortium for outcome measures and biomarkers for neurodevelopmental disorders. We are collaborating to cure rare, non-verbal brain disorders.
Moonshots for Unicorns
Curing single-gene disorders
Project CASK
To fund research for treatment and/or a cure for CASK Gene Disorder
Clinical Trials
For a list of clinical trials in this disease area, please click here.