Lateral meningocele syndrome
Synonyms: Lehman syndrome
A rare genetic neurological disorder characterized by multiple lateral meningoceles distinctive facial dysmorphism (including hypertelorism downslanting palpebral fissures posteriorly rotated ears micrognathia and high narrow palate among others) and skeletal abnormalities (e. g. vertebral anomalies wormian bones short stature and scoliosis). Multiple additional features may present such as conductive hearing impairment hypotonia and connective tissue and urogenital abnormalities. Cognition is usually normal.
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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Lateral meningocele syndrome?
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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
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.