Results 51 to 60 of about 220,579 (147)

HETEROTOPIA — DISJUNCTURE II [PDF]

open access: yes
Artist and curator Paul Jones continues the exploration of liminal spaces, separate from but parallel with reality. The first iteration of HETEROTOPIA — DISJUNCTURE took place in 2022 at 19a Parade Mews, London. Presenting the work of 6 international
Jones, Paul
core   +5 more sources

KBG syndrome: A scoping review of electroclinical features of patients with epilepsy

open access: yesEpileptic Disorders, EarlyView.
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini   +6 more
wiley   +1 more source

Carrier screening in the reproductive setting—Are there medical implications for the heterozygote?—A guide for clinicians

open access: yesPregnancy, Volume 2, Issue 3, May 2026.
Abstract Carrier screening for genetic conditions performed preconception or during pregnancy allows identification of fetal risk for inherited autosomal recessive and X‐linked conditions. The goal is to identify at‐risk patients/couples and offer them reproductive options such as preimplantation genetic diagnosis, prenatal testing, or targeted newborn
Emily B. Rosenfeld   +5 more
wiley   +1 more source

Nasal glial heterotopia – Clinical manifestation in 2.5 month-old boy [PDF]

open access: yes, 2019
Nasal glial heterotopia is a rare congenital defect that is formed during embryonic development. This lesion is a part of a larger group of diseases, congenital midline nasal tumors, that occur with a frequency of one per 20,000-40,000 live births ...
Szydłowski, Jarosław   +5 more
core  

International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors

open access: yesInternational Forum of Allergy &Rhinology, Volume 14, Issue 2, Page 149-608, February 2024.
Abstract Background Sinonasal neoplasms, whether benign and malignant, pose a significant challenge to clinicians and represent a model area for multidisciplinary collaboration in order to optimize patient care. The International Consensus Statement on Allergy and Rhinology: Sinonasal Tumors (ICSNT) aims to summarize the best available evidence and ...
Edward C. Kuan   +158 more
wiley   +1 more source

Combined approach of transnasal and transoral endoscopic surgery in a child with nasal glial heterotopia; Przeznosowy i przezustny dostęp endoskopowy u dziecka z nosową heterotopią glejową

open access: yes, 2022
Aim of the study: The aim of this case report is to outline the difficulties associated with managing a child with nasal glial heterotopia. Developmental midline nasal mass, especially of neurogenic origin, poses a great challenge to managing surgeons ...
Saniasiaya, Jeyasakthy   +4 more
core  

Nasal heterotopia versus pilocytic astrocytoma: A narrow border.

open access: yes, 2015
peer reviewedFailure of the anterior neuropore can lead to three main types of anomalies: nasal dermal sinus, encephalocele and nasal glioma or heterotopia.
Piette, Caroline   +6 more
core   +1 more source

Glial Heterotopia of the orbit: A rare presentation [PDF]

open access: yes, 2011
Background Glial heterotopias are rare, benign, congenital, midline, non-teratomatous extracranial glial tissue. They may masquerade as encephalocoele or dermoid cyst and mostly present in nose.
Shah Dev N   +9 more
core   +2 more sources

Case Report - Extranasal glial heterotopia: Case report

open access: yes, 2003
Glial heterotopia or the occurrence of isolated non-teratomatous extracranial glial tissue is rare. We report a neonate with extensive extranasal glial heterotopia involving the left buccopharyngeal region, palate and base of the skull and presenting ...
S. Mohanty   +3 more
core   +2 more sources

Oropharyngeal neuroglial heterotopia/choristoma with intracranial and extra-oral extension: A case report

open access: yesOtolaryngology Case Reports
Background: Neuroglial heterotopia, also referred to as glial choristoma, is a rare congenital malformation characterized by ectopic glial tissue outside the central nervous system.
Yara A. Akkielah   +8 more
doaj   +1 more source

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