ArticleNeuroradiology2004
Pituitary duplication associated with oral dermoid and corpus callosum hypogenesis.
Article in Neuroradiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
8 citing papers in PubMed.
- New patients with duplication of the pituitary gland-plus syndrome, including aJournal of medical genetics · 2025Review
- Duplication of the Pituitary Gland (DPG)-Plus Syndrome Associated With Midline Anomalies and Precocious Puberty: A Case Report and Review of the Literature.Frontiers in endocrinology · 2021Review
- DPG-plus syndrome: new report of a rare entity.BMJ case reports · 2015Article
- CT and MRI of congenital nasal lesions in syndromic conditions.Pediatric radiology · 2015Review
- Duplication of the pituitary gland associated with multiple blastogenesis defects: Duplication of the pituitary gland (DPG)-plus syndrome. Case report and review of literature.Surgical neurology international · 2012Article
- Pituitary duplication: a rare cause of precocious puberty.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2011Article
- Lack of the ventral anterior homeodomain transcription factor VAX1 leads to induction of a second pituitary.Development (Cambridge, England) · 2011Article
- UNIQUE PRESENTATION OF DUPLICATION OF THE PITUITARY GLAND-PLUS SYNDROME.AACE clinical case reportsArticle
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
We report a case of pituitary duplication in a neonate girl whose magnetic resonance (MR) images showed unusual findings of hypogenesis of the corpus callosum and oral dermoid. Pituitary duplication is an extremely rare malformation, with only a few previously reported cases. It occurs most commonly in association with complicated midline and skull base anomalies. We present a case of this malformation with special emphasis on the hypogenesis of splenium of the corpus callosum and oral dermoid.
Indexed as
Identifiers
15565346What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.