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Encephalocele

More information in Books or onNLM PubMed
Definition: Brain tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur.  meningoencephalocele: coordinate IM with MENINGOCELE (IM)    Other names Occipital Encephalocele; Hernia, Cerebral; Frontal Encephalocele; Tonsillar Herniations; Tonsillar Hernias; Sincipital Encephaloceles; Occipital Encephaloceles; Notoencephaloceles; Meningoencephaloceles, Cranial; Meningoencephalocele, Cranial; Herniations, Tonsillar; Herniations, Cerebellar; Herniation, Tonsillar; Herniation, Cerebellar; Hernias, Tonsillar; Hernias, Cerebral; Hernias, Cerebellar; Hernia, Tonsillar; Hernia, Cerebellar; Frontal Encephaloceles
 
SubstanceCAS Registry & nameCategoriesSource
Knobloch Syndrome Type III  0   *Encephalocele *Retinal Detachment/congenital.
Knobloch Syndrome Type II  0   *Encephalocele *Retinal Detachment/congenital.
Fronto-facio-nasal dysplasia  0   *Encephalocele *Eye Abnormalities *Facial Asymmetry *Craniofacial Abnormalities Nose/abnormalities.
Podder-Tolmie syndrome  0   *Abnormalities, Multiple *Arthrogryposis *Encephalocele Thumb/abnormalities.
Knobloch syndrome  0   *Encephalocele *Retinal Detachment/congenital.
Meckel syndrome type 1  0   *Ciliary Motility Disorders *Encephalocele *Polycystic Kidney Diseases.
Meckel syndrome type 3  0   *Ciliary Motility Disorders *Encephalocele *Polycystic Kidney Diseases.
Meckel syndrome type 2  0   *Ciliary Motility Disorders *Encephalocele *Polycystic Kidney Diseases.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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