About 15 results

ALLMedicine™ Absence Of Septum Pellucidum Center

Research & Reviews  6 results

Rhomboencephalosynapsis: Review of the Literature.
World Neurosurgery; Fouda MA, Kim TY et. al.

Dec 27th, 2021 - Rhombencephalosynapsis is a rare congenital anomaly, characterized by partial or total agenesis of the cerebellar vermis with midline fusion of the cerebellar hemispheres, dentate nuclei, and the superior cerebellar peduncles, creating the distinc...

Septo-optic dysplasia with amniotic band syndrome sequence: a case report.
Journal of Medical Case Reports; Amiji IA, Mohamed UH et. al.

Dec 17th, 2019 - De Morsier syndrome, or septo-optic dysplasia, is a rare, heterogeneous, complex condition with a highly variable phenotype. It is characterized by optic nerve hypoplasia, pituitary gland hypoplasia, and midline brain abnormalities, including abse...

Holoprosencephaly or severe hydrocephalus: T1 sequence tells the story.
BMJ Case Reports; Zarei F, Iranpour P et. al.

May 10th, 2019 - Intracranial lipoma is a relatively rare benign lesion. Many are incidental findings; however, some others may present with headache, hydrocephalus or other neurological symptoms; thus, correct diagnosis of this condition is important. These lesio...

Absence of septum pellucidum

Nov 19th, 2016 - The absence of the septum pellucidum is a rare condition that affects the structure of the brain. Specifically, a thin membrane called the septum pellucidum is missing from its normal position in the middle of the brain.[1] When it is missing, sym...

Isolated absence of septum pellucidum: prenatal diagnosis and outcome.
Fetal Diagnosis and Therapy; García-Arreza A, García-Díaz L et. al.

May 11th, 2012 - Septal agenesis is a rare cerebral developmental anomaly characterized by partial or complete absence of the septum pellucidum (ASP). Septal agenesis may be associated with various congenital brain malformations, namely holoprosencephaly, septoopt...

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