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Child's Nervous System
Erschienen in: Child's Nervous System 5/2020

05.03.2020 | Review Article

The development of vision between nature and nurture: clinical implications from visual neuroscience

verfasst von: Giulia Purpura, Francesca Tinelli

Erschienen in: Child's Nervous System | Ausgabe 5/2020

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Abstract

Background

Vision is an adaptive function and should be considered a prerequisite for neurodevelopment because it permits the organization and the comprehension of the sensory data collected by the visual system during daily life. For this reason, the influence of visual functions on neuromotor, cognitive, and emotional development has been investigated by several studies that have highlighted how visual functions can drive the organization and maturation of human behavior. Recent studies on animals and human models have indicated that visual functions mature gradually during post-natal life, and its development is closely linked to environment and experience.

Discussion

The role of vision in early brain development and some of the neuroplasticity mechanisms that have been described in the presence of cerebral damage during childhood are analyzed in this review, according to a neurorehabilitation prospective.
Literatur
1.
Barca L, Cappelli FR, di Giulio P, Staccioli S, Castelli E (2010) Outpatient assessment of neurovisual functions in children with cerebral palsy. Res Dev Disabil 31(2):488–495PubMed
2.
3.
Baroncelli L, Braschi C, Spolidoro M, Begenisic T, Sale A, Maffei L (2010) Nurturing brain plasticity: impact of environmental enrichment. Cell Death Differ 17(7):1092–1103PubMed
4.
Mercuri E et al (2007) The development of vision. Early Hum Dev 83(12):795–800PubMed
5.
Braddick O, Atkinson J (2011) Development of human visual function. Vis Res 51(13):1588–1609PubMed
6.
Atkinson J (1984) Human visual development over the first 6 months of life. A review and a hypothesis. Hum Neurobiol 3(2):61–74PubMed
7.
Spillmann L (2014) Receptive fields of visual neurons: the early years. Perception 43(11):1145–1176PubMed
8.
9.
Berardi N, Pizzorusso T, Ratto GM, Maffei L (2003) Molecular basis of plasticity in the visual cortex. Trends Neurosci 26(7):369–378PubMed
10.
May A, Hajak G, Gänssbauer S, Steffens T, Langguth B, Kleinjung T, Eichhammer P (2007) Structural brain alterations following 5 days of intervention: dynamic aspects of neuroplasticity. Cereb Cortex 17(1):205–210PubMed
11.
Nabel EM, Morishita H (2013) Regulating critical period plasticity: insight from the visual system to fear circuitry for therapeutic interventions. Front Psychiatry 4:146PubMedPubMedCentral
12.
Morrone MC (2010) Brain development: critical periods for cross-sensory plasticity. Curr Biol 20(21):R934–R936PubMed
13.
Daw NW (1998) Critical periods and amblyopia. Arch Ophthalmol 116(4):502–505PubMed
14.
Kiorpes L (2015) Visual development in primates: neural mechanisms and critical periods. Dev Neurobiol 75(10):1080–1090PubMedPubMedCentral
15.
16.
Kupers R, Ptito M (2014) Compensatory plasticity and cross-modal reorganization following early visual deprivation. Neurosci Biobehav Rev 41:36–52PubMed
17.
Merabet LB, Pascual-Leone A (2010) Neural reorganization following sensory loss: the opportunity of change. Nat Rev Neurosci 11(1):44–52PubMed
18.
Werth R (2008) Cerebral blindness and plasticity of the visual system in children. A review of visual capacities in patients with occipital lesions, hemispherectomy or hydranencephaly. Restor Neurol Neurosci 26(4–5):377–389PubMed
19.
20.
Cancedda L et al (2004) Acceleration of visual system development by environmental enrichment. J Neurosci 24(20):4840–4848PubMedPubMedCentral
21.
Guzzetta A, Baldini S, Bancale A, Baroncelli L, Ciucci F, Ghirri P, Putignano E, Sale A, Viegi A, Berardi N, Boldrini A, Cioni G, Maffei L (2009) Massage accelerates brain development and the maturation of visual function. J Neurosci 29(18):6042–6051PubMedPubMedCentral
22.
Purpura G, Tinelli F, Bargagna S, Bozza M, Bastiani L, Cioni G (2014) Effect of early multisensory massage intervention on visual functions in infants with down syndrome. Early Hum Dev 90(12):809–813PubMed
23.
Baroncelli L, Sale A, Viegi A, Maya Vetencourt JF, de Pasquale R, Baldini S, Maffei L (2010) Experience-dependent reactivation of ocular dominance plasticity in the adult visual cortex. Exp Neurol 226(1):100–109PubMed
24.
Berardi N, Pizzorusso T, Maffei L (2000) Critical periods during sensory development. Curr Opin Neurobiol 10(1):138–145PubMed
25.
Sugita Y (2009) Innate face processing. Curr Opin Neurobiol 19(1):39–44PubMed
26.
Simion F, Leo I, Turati C, Valenza E, Dalla Barba B (2007) How face specialization emerges in the first months of life. Prog Brain Res 164:169–185PubMed
27.
Valenza E, Simion F, Cassia VM, Umiltà C (1996) Face preference at birth. J Exp Psychol Hum Percept Perform 22(4):892–903PubMed
28.
Fraiberg S (1977) Insights from the blind. Basic Books, New York
29.
Land MF (2006) Eye movements and the control of actions in everyday life. Prog Retin Eye Res 25(3):296–324PubMed
30.
Hood B, Atkinson J (1990) Sensory visual loss and cognitive deficits in the selective attentional system of normal infants and neurologically impaired children. Dev Med Child Neurol 32(12):1067–1077PubMed
31.
Tadic V, Pring L, Dale N (2010) Are language and social communication intact in children with congenital visual impairment at school age? J Child Psychol Psychiatry 51(6):696–705PubMed
32.
Prechtl HF, Cioni G, Einspieler C, Bos AF, Ferrari F (2001) Role of vision on early motor development: lessons from the blind. Dev Med Child Neurol 43(3):198–201PubMed
33.
Braddick O, Atkinson J (2013) Visual control of manual actions: brain mechanisms in typical development and developmental disorders. Dev Med Child Neurol 55(Suppl 4):13–18PubMed
34.
Babinsky E, Braddick O, Atkinson J (2012) Infants and adults reaching in the dark. Exp Brain Res 217(2):237–249PubMed
35.
Hallemans A, Ortibus E, Truijen S, Meire F (2011) Development of independent locomotion in children with a severe visual impairment. Res Dev Disabil 32(6):2069–2074PubMed
36.
Dale N, Sakkalou E, O'Reilly M, Springall C, de Haan M, Salt A (2017) Functional vision and cognition in infants with congenital disorders of the peripheral visual system. Dev Med Child Neurol 59(7):725–731PubMed
37.
Mercuri E, Haataja L, Guzzetta A, Anker S, Cowan F, Rutherford M, Andrew R, Braddick O, Cioni G, Dubowitz L, Atkinson J (1999) Visual function in term infants with hypoxic-ischaemic insults: correlation with neurodevelopment at 2 years of age. Arch Dis Child Fetal Neonatal Ed 80(2):F99–F104
38.
Guzzetta A, Mazzotti S, Tinelli F, Bancale A, Ferretti G, Battini R, Bartalena L, Boldrini A, Cioni G (2006) Early assessment of visual information processing and neurological outcome in preterm infants. Neuropediatrics 37(5):278–285
39.
Cass HD, Sonksen PM, McConachie HR (1994) Developmental setback in severe visual impairment. Arch Dis Child 70(3):192–196PubMedPubMedCentral
40.
Dale N, Sonksen P (2002) Developmental outcome, including setback, in young children with severe visual impairment. Dev Med Child Neurol 44(9):613–622PubMed
41.
Fazzi E et al (2007) Leber’s congenital amaurosis: is there an autistic component? Dev Med Child Neurol 49(7):503–507PubMed
42.
Do B et al (2017) Systematic review and meta-analysis of the association of autism spectrum disorder in visually or hearing impaired children. Ophthalmic Physiol Opt 37(2):212–224PubMed
43.
Mukaddes NM, Kilincaslan A, Kucukyazici G, Sevketoglu T, Tuncer S (2007) Autism in visually impaired individuals. Psychiatry Clin Neurosci 61(1):39–44PubMed
44.
Bathelt J, de Haan M, Dale NJ (2019) Adaptive behaviour and quality of life in school-age children with congenital visual disorders and different levels of visual impairment. Res Dev Disabil 85:154–162PubMed
45.
46.
Ricci D, Romeo DM, Gallini F, Groppo M, Cesarini L, Pisoni S, Serrao F, Papacci P, Contaldo I, Perrino F, Brogna C, Bianco F, Baranello G, Sacco A, Quintiliani M, Ometto A, Cilauro S, Mosca F, Romagnoli C, Romeo MG, Cowan F, Cioni G, Ramenghi L, Mercuri E (2011) Early visual assessment in preterm infants with and without brain lesions: correlation with visual and neurodevelopmental outcome at 12 months. Early Hum Dev 87(3):177–182PubMed
47.
Guzzetta A, D’Acunto G, Rose S, Tinelli F, Boyd R, Cioni G (2010) Plasticity of the visual system after early brain damage. Dev Med Child Neurol 52(10):891–900PubMed
48.
Matsuba C, Soul J (2010) Clinical manifestation of cerebral visual impairment. In: Dutton GN, Bax M (eds) visual impairment in children due to damage to the brain. Mac Keith Press, London
49.
Guzzetta A, Fazzi B, Mercuri E, Bertuccelli B, Canapicchi R, van Hof-van Duin J, Cioni G (2001) Visual function in children with hemiplegia in the first years of life. Dev Med Child Neurol 43(5):321–329PubMed
50.
Zihl J (1995) Visual scanning behavior in patients with homonymous hemianopia. Neuropsychologia 33(3):287–303PubMed
51.
Cowey A (2010) The blindsight saga. Exp Brain Res 200(1):3–24PubMed
52.
Stoerig P, Cowey A (2007) Blindsight. Curr Biol 17(19):R822–R824PubMed
53.
Weiskrantz L (1996) Blindsight revisited. Curr Opin Neurobiol 6(2):215–220PubMed
54.
Cowey A, Stoerig P (1991) The neurobiology of blindsight. Trends Neurosci 14(4):140–145PubMed
55.
Tinelli F, Guzzetta A, Bertini C, Ricci D, Mercuri E, Ladavas E, Cioni G (2011) Greater sparing of visual search abilities in children after congenital rather than acquired focal brain damage. Neurorehabil Neural Repair 25(8):721–728PubMed
56.
Muckli L, Naumer MJ, Singer W (2009) Bilateral visual field maps in a patient with only one hemisphere. Proc Natl Acad Sci U S A 106(31):13034–13039PubMedPubMedCentral
57.
Tinelli F, Cicchini GM, Arrighi R, Tosetti M, Cioni G, Morrone MC (2013) Blindsight in children with congenital and acquired cerebral lesions. Cortex 49(6):1636–1647PubMed
58.
Ptito A, Leh SE (2007) Neural substrates of blindsight after hemispherectomy. Neuroscientist 13(5):506–518PubMed
59.
Sahraie A, Hibbard PB, Trevethan CT, Ritchie KL, Weiskrantz L (2010) Consciousness of the first order in blindsight. Proc Natl Acad Sci U S A 107(49):21217–21222PubMedPubMedCentral
60.
Bourne JA, Morrone MC (2017) Plasticity of visual pathways and function in the developing brain: is the Pulvinar a crucial player? Front Syst Neurosci 11:3PubMedPubMedCentral
61.
Payne BR, Lomber SG, Macneil MA, Cornwell P (1996) Evidence for greater sight in blindsight following damage of primary visual cortex early in life. Neuropsychologia 34(8):741–774PubMed
62.
Sorenson KM, Rodman HR (1999) A transient geniculo-extrastriate pathway in macaques? Implications for ‘blindsight’. Neuroreport 10(16):3295–3299PubMed
63.
Lyon DC, Nassi JJ, Callaway EM (2010) A disynaptic relay from superior colliculus to dorsal stream visual cortex in macaque monkey. Neuron 65(2):270–279PubMedPubMedCentral
64.
Tomaiuolo F et al (1997) Blindsight in hemispherectomized patients as revealed by spatial summation across the vertical meridian. Brain 120(Pt 5):795–803PubMed
65.
Tamietto M, Cauda F, Corazzini LL, Savazzi S, Marzi CA, Goebel R, Weiskrantz L, de Gelder B (2010) Collicular vision guides nonconscious behavior. J Cogn Neurosci 22(5):888–902PubMed
66.
Ajina S, Bridge H (2018) Subcortical pathways to extrastriate visual cortex underlie residual vision following bilateral damage to V1. Neuropsychologia 128:140–149PubMed
67.
Ajina S et al (2015) Human blindsight is mediated by an intact geniculo-extrastriate pathway. Elife 4
68.
Mikellidou K, Frijia F, Montanaro D, Greco V, Burr DC, Morrone MC (2018) Cortical BOLD responses to moderate- and high-speed motion in the human visual cortex. Sci Rep 8(1):8357PubMedPubMedCentral
69.
Mikellidou K, Arrighi R, Aghakhanyan G, Tinelli F, Frijia F, Crespi S, de Masi F, Montanaro D, Morrone MC (2019) Plasticity of the human visual brain after an early cortical lesion. Neuropsychologia 128:166–177PubMed
70.
Warraich Z, Kleim JA (2010) Neural plasticity: the biological substrate for neurorehabilitation. PM R 2(12 Suppl 2):S208–S219PubMed
71.
Hensch TK, Bilimoria PM (2012) Re-opening windows: manipulating critical periods for brain development. Cerebrum 2012:11PubMedPubMedCentral
72.
Johnston C, Cossette S, Archer J, Ranger M, Nahas-Chebli G (2009) Developing synergy to enhance the impact of nursing intervention research on patient health. Can J Nurs Res 41(4):115–121PubMed
73.
Dale NJ, Sakkalou E, O'Reilly MA, Springall C, Sakki H, Glew S, Pissaridou E, de Haan M, Salt AT (2019) Home-based early intervention in infants and young children with visual impairment using the developmental journal: longitudinal cohort study. Dev Med Child Neurol 61(6):697–709PubMed
Metadaten
Titel
The development of vision between nature and nurture: clinical implications from visual neuroscience
verfasst von
Giulia Purpura
Francesca Tinelli
Publikationsdatum
05.03.2020
Verlag
Springer Berlin Heidelberg
Erschienen in
Child's Nervous System / Ausgabe 5/2020
Print ISSN: 0256-7040
Elektronische ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-020-04554-1

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