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ALLMedicine™ Absence Of Septum Pellucidum Center

Research & Reviews  6 results

Septo-optic dysplasia with amniotic band syndrome sequence: a case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913001
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.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6506112
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
https://rarediseases.info.nih.gov/diseases/9253/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.
https://doi.org/10.1159/000338009
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...

A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome.
https://doi.org/10.1002/ajmg.a.33308
American Journal of Medical Genetics. Part A; Pacanaro AN, Christofolini DM et. al.

Feb 27th, 2010 - Supernumerary marker chromosomes (sSMC) may or may not be associated with an abnormal phenotype, depending on the presence of euchromatin, on their chromosomal origin and whether they are inherited. Over 80% of sSMCs are derived from acrocentric c...

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