Dendritic arborization in the human fetus and infant with the trisomy 18 syndrome
Abstract
Dendritic arborization patterns of visual cortical neurons in four cases of trisomy 18 syndrome were compared with those in 8 neurologically asymptomatic age-matched controls. The trisomy cases included a 20-week-old fetus, a term infant, a 3-month-old infant, and 6-month-old infant. Quantitative Golgi analysis showed a decrease in the mean total dendritic length of apical dendrites in layer 5 pyramidal neurons in the term infant with trisomy 18. In layer 3, an attenuated dendritic tree was observed in the earlier age groups with increased dendritic extent at 6 months. Although not conclusive, due to the small number of subjects, this preliminary study showed definitive dendritic abnormalities in the trisomy 18 syndrome.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In all human chromosomal aberration syndromes, including trisomies, monosomies, polyploidies, disomies and imprinting errors or sex chromosome anomalies, structural abnormalities of (pre)frontal as well as many other areas are common.
“In all human chromosomal aberration syndromes, including trisomies, monosomies (e.g., Turner syndrome, monosomy 1p36), polyploidies, disomies and imprinting errors or sex chromosome anomalies, structural abnormalities of (pre)frontal as well as many other areas are common [61, 288–292].”
From Development of prefrontal cortex (2022) · cites this paper as [291]
Cites
Edwards, J., Harnden, D. G., Cameron, A., Crosse, V. M., & Wolf, O. H. (1960) · The Lancet · doi:10.1016/s0140-6736(60)90675-9 · Cited by 628 · see citing works
Dendritic Spine "Dysgenesis" and Mental Retardation
Purpura, D. P. (1974) · Science · doi:10.1126/science.186.4169.1126 · Cited by 522 · see citing works
McCracken, G. H., Mize, S. G., & Threlkeld, N. (1980) · PubMed · Cited by 393 · see citing works
Takashima, S., Becker, L. E., Armstrong, D. L., & Chan, F. (1981) · Brain Research · doi:10.1016/0006-8993(81)90314-0 · Cited by 307 · see citing works
Self-citationStructural abnormalities of the cerebral cortex in human chromosomal aberrations: a Golgi study
Marin-Padilla, M. (1972) · Brain Research · doi:10.1016/0006-8993(72)90324-1 · Cited by 290 · see citing works
Dendritic atrophy in children with down’s syndrome.
Becker, L. E., Armstrong, D. L., & Chan, F. (1986) · Annals of Neurology · doi:10.1002/ana.410200413 · Cited by 279 · see citing works
Self-citationCongenital and acquired cognitive disorders
Comings, D. E. (1979) · Europe PMC (PubMed Central) · Cited by 199 · see citing works
Normal and Aberrant Neuronal Development in the Cerebral Cortex of Human Fetus and Young Infant
Purpura, D. P. (1975) · Elsevier eBooks · doi:10.1016/b978-0-12-139050-1.50014-8 · Cited by 134 · see citing works
Williams, R. S., Ferrante, R. J., & Caviness, V. S. (1978) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-197801000-00002 · Cited by 131 · see citing works
Brain mechanisms in mental retardation
Spehlmann, R. (1976) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(76)90016-x · Cited by 124 · see citing works
Dendritic development in human occipital cortical neurons
Becker, L. E., Armstrong, D. L., Chan, F., & Wood, M. M. (1984) · Developmental Brain Research · doi:10.1016/0165-3806(84)90083-x · Cited by 112 · see citing works
Self-citationMarín‐Padilla, M. (1974) · Brain Research · doi:10.1016/0006-8993(74)90054-7 · Cited by 111 · see citing works
Morphology of the Developing Visual Cortex of the Human Infant
Takashima, S., Chan, F.-W., Becker, L. E., & ARMSTRONG, D. L. (1980) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-198007000-00007 · Cited by 108 · see citing works
Self-citationMalformations of the central nervous system in trisomy 18 syndrome
Passarge, E., True, C. W., Sueoka, W. T., et al. (1966) · The Journal of Pediatrics · doi:10.1016/s0022-3476(66)80123-3 · Cited by 53 · see citing works
Synaptic and Dendritic Development and Mental Defect
Huttenlocher, P. R. (1975) · Elsevier eBooks · doi:10.1016/b978-0-12-139050-1.50013-6 · Cited by 51 · see citing works
Central nervous system abnormalities in Trisomy E (17–18) syndrome
Michaelson, P. S., & Gilles, F. H. (1972) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(72)90007-x · Cited by 26 · see citing works
Histologic Structural Anomalies in the Brain in Trisomy 18 Syndrome
TERPLAN, K. L. (1970) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1970.02100050230008 · Cited by 20 · see citing works
The neuropathology of the 17-18 trisomy syndrome.
Kakulas, B. A., Hr, T., Cullity, G. J., et al. (1968) · PubMed · Cited by 7 · see citing works
Cerebellar Changes in Association With "Partial" Trisomy 18
TERPLAN, K. L. (1968) · Archives of Pediatrics and Adolescent Medicine · doi:10.1001/archpedi.1968.02100010181005 · Cited by 6 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Development of prefrontal cortex
Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378 · see citing works
A human neurodevelopmental model for Williams syndrome
Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature · doi:10.1038/nature19067 · Cited by 195 · see citing works
Hrvoj-Mihic, B., Hanson, K. L., Lew, C. H., Stefanacci, L., Jacobs, B., Bellugi, U., & Semendeferi, K. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00419 · Cited by 21 · see citing works
- Authors
- Jay, V., Chan, F.-W., & Becker, L. E.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Becker, Laurence E.
- Venue
- Developmental Brain Research
- Publisher
- Elsevier BV
- Published
- 1990-07
- Volume
- 54
- Issue
- 2
- Pages
- 291-294
- ISSN
- 0165-3806 (ISSN-L)
- OpenAlex
- W2094196257
- Cited by
- 10
- References
- 19
- Citations by year
- 2021: 2 · 2017: 1 · 2016: 1 · 2014: 1 · 2013: 1
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Developmental Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Fetal and Pediatric Neurological Disorders
- Keywords
- trisomy 18, trisomy 13, dendritic branching, dendritic length, visual cortex, pyramidal neurons, layer 5, layer 3, human fetus, infant brain development, Golgi staining
- MeSH terms
- Chromosomes, Human, Pair 18, Dendrites, Fetus, Humans, Syndrome, Trisomy, Visual Cortex
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review