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Books on the topic 'Neurocutaneous Disorders'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Panteliadis, Christos P., Ramsis Benjamin, and Christian Hagel, eds. Neurocutaneous Disorders. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-87893-1.

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2

S, Roach E., and Miller Van S, eds. Neurocutaneous disorders. Cambridge University Press, 2004.

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Ruggieri, Martino, Ignacio Pascual-Castroviejo, and Concezio Di Rocco, eds. Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes. Springer Vienna, 2008. http://dx.doi.org/10.1007/978-3-211-69500-5.

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4

Bertrand, Carrie. Awareness: Morgellons. AuthorHouse, 2009.

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5

Conroy, David. Morgellon's syndrome: Evidence of a microorganism causing an unexplained dermopathy. Science Publishers, 2009.

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6

Roach, E. Steve, and Van S. Miller. Neurocutaneous Disorders. Cambridge University Press, 2006.

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7

Neurocutaneous Disorders. Elsevier, 2016. http://dx.doi.org/10.1016/c2015-0-00737-7.

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8

Roach, E. Steve, and Van S. Miller, eds. Neurocutaneous Disorders. Cambridge University Press, 2004. http://dx.doi.org/10.1017/cbo9780511545054.

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9

Roach, E. S., and Van S. Miller. Neurocutaneous Disorders. Cambridge University Press, 2004.

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10

Roach, E. Steve, and Van S. Miller. Neurocutaneous Disorders. Cambridge University Press, 2004.

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11

Roach, E. Steve, and Van S. Miller. Neurocutaneous Disorders. Cambridge University Press, 2004.

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12

Roach, E. Steve, and Van S. Miller. Neurocutaneous Disorders. University of Cambridge ESOL Examinations, 2009.

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13

Talati, Asha N., and David N. Hackney. Neurocutaneous Disorders in Pregnancy. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190667351.003.0028.

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Neurocutaneous disorders are rare genetic conditions that can produce malformations of skin and various organ systems. During pregnancy, such conditions often require a specific course of management with coordinated care between neurology, obstetrics, and neonatology in order to promote best maternal and fetal outcomes. This chapter reviews the most common neurocutaneous conditions and best practices for management of these conditions in pregnancy. Neurocutaneous conditions discussed in this chapter include neurofibromatosis types I and II, Ehlers Danlos syndrome, Tuberous Sclerosis, Von Hippe

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14

Rocco, Concezio Di, Martino Ruggieri, and Ignacio Pascual Castroviejo. Neurocutaneous Disorders: Phakomatoses & Hamartoneoplastic Syndromes. Springer, 2016.

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15

(Editor), Martino Ruggieri, Ignacio Pascual Castroviejo (Editor), and Concezio Di Rocco (Editor), eds. Neurocutaneous Disorders: Phakomatoses & Hamartoneoplastic Syndromes. Springer, 2008.

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16

Rocco, Concezio Di, Martino Ruggieri, and Ignacio Pascual Castroviejo. Neurocutaneous Disorders: Phakomatoses and Hamartoneoplastic Syndromes. Springer London, Limited, 2009.

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17

Grant, Robert. Neurocutaneous syndromes. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569381.003.0235.

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This chapter describes several neurocutaneous syndromes, including tuberous sclerosis, neurofibromatosis, Sturge–Weber syndrome, Von-Hippel–Lindau disease and ataxia telangiectasia amongst others.Tuberous sclerosis, also known as Epiloia or Bournville’s Disease, is an autosomal dominant multisystem disease it usually presents in childhood with a characteristic facial rash, adenoma sebaceum, seizures, and sometimes learning difficulties. Central nervous system lesions in tuberous sclerosis are due to a developmental disorder of neurogenesis and neuronal migration. Other organs such as the heart

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18

Jordan, Nerissa. Neurocutaneous syndromes. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0224.

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The neurocutaneous syndromes comprise a diverse group of rare genetic disorders with both neurological and cutaneous manifestations. Each syndrome has a distinct phenotype. Symptoms are variable and depend on the syndrome. Neurocutaneous syndromes often present in childhood or adolescence; for example, tuberous sclerosis typically presents in early childhood. The age range of presentation is broad, depending on the specific condition and severity of expression. The majority are autosomally inherited conditions. De novo mutations can occur. Most neurocutaneous syndromes do not have a specific t

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19

Panteliadis, Christos P., Ramsis Benjamin, and Christian Hagel. Neurocutaneous Disorders: A Clinical, Diagnostic and Therapeutic Approach. Springer International Publishing AG, 2021.

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20

Panteliadis, Christos P., Ramsis Benjamin, and Christian Hagel. Neurocutaneous Disorders: A Clinical, Diagnostic and Therapeutic Approach. Urban & Fischer Verlag GmbH & Co. KG, 2016.

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21

Neurocutaneous Disorders: A Clinical, Diagnostic and Therapeutic Approach. Springer International Publishing AG, 2023.

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22

Christos P., M.D. Panteliadis (Editor), Ramsis, M.D. Benjamin (Editor), Hansjorg, M.D., Ph.D. Cremer (Editor), Christian, M.D., Ph.D. Hagel (Editor), and Heymut, M.D. Omran (Editor), eds. Neurocutaneous Disorders - Hemangiomas: A Clinical and Diagnostic Approach. Anshan Publishing, 2007.

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23

Gaitanis, John, Phillip L. Pearl, and Howard Goodkin. The EEG in Degenerative Disorders of the Central Nervous System. Edited by Donald L. Schomer and Fernando H. Lopes da Silva. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190228484.003.0013.

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Nervous system alterations can occur at any stage of prenatal or postnatal development. Any of these derangements, whether environmental or genetic, will affect electrical transmission, causing electroencephalogram (EEG) alteration and possibly epilepsy. Genetic insults may be multisystemic (for example, neurocutaneous syndromes) or affect only the brain. Gene mutations account for inborn errors of metabolism, channelopathies, brain malformations, and impaired synaptogenesis. Inborn errors of metabolism cause seizures and EEG abnormalities through a variety of mechanisms, including disrupted e

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24

Ulnik, Jorge. Skin in Psychoanalysis. Taylor & Francis Group, 2020.

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25

Ulnik, Jorge. Skin in Psychoanalysis. Taylor & Francis Group, 2020.

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26

Legido, Agustin, and Joseph H. Piatt. Clinical Pediatric Neurosciences for Primary Care. American Academy of Pediatrics, 2005. http://dx.doi.org/10.1542/9781581104325.

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This all-new clinical resource equips primary caregivers to take a lead role in the diagnosis, evaluation, and management of diverse pediatric neurologic and neurosurgical conditions. For practice-focused guidance with a coordinated dual perspective you won't find anywhere else. The developers/editors are a pediatric neurologist and a pediatric neurosurgeon at the forefront of their fields. Key topics are considered from neurologic and neurosurgical viewpoints. Purpose-built for efficient clinical problem solving; clear, concise overviews of a broad range of common conditions; evidence-based d

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27

Ehninger, Dan, and Alcino J. Silva. Tuberous Sclerosis and Autism. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199744312.003.0009.

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Tuberous sclerosis (TSC) is a single-gene disorder caused by heterozygous mutations in either the TSC1 or TSC2 genes (Consortium, 1993; van Slegtenhorst et al., 1997). In 70% of cases, TSC gene mutations arise de novo. The remaining 30% of cases are familial with an autosomal dominant pattern of inheritance. Tuberous sclerosis belongs to the group of phakomatoses (neurocutaneous disorders) and is associated with characteristic manifestations in various organ systems, including the brain, skin, kidney, lung, heart, and liver (Crino, Nathanson, & Henske, 2006; Curatolo, Bombardieri & Joz

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28

Forsyth, Rob, and Richard Newton. Specific conditions. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198784449.003.0004.

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This chapter adopts a systematic approach to common diagnoses in paediatric neurology, aetiologies, management to include investigation and treatment, and outcome. For each condition current knowledge on cause and underlying biology is summarized. A rational approach to investigation and treatment is summarized for each topic. These include: acquired brain injury; autoimmune and autoinflammatory disease of the CNS; cerebral palsy and neurodisability which covers feeding, communication, special senses, and respiratory disease; demyelinating disease; epilepsy including its impact on daily life;

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29

Shaibani, Aziz. Skin Signs. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199898152.003.0027.

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Many neuromuscular diseases are expressed by skin manifestations such as dermatomyositis. Skin changes of dermatomyositis are of many types and can be subtle in dark skin. Skin rash may be the only finding in dermatomyositis (amyopathic dermatomyositis). Many systemic inflammatory diseases are associated with skin lesions and neuromuscular involvement such as vasculitis, SLE, and scleroderma. Steroids may lead to acne-like skin lesions that should be differentiated from the rash of the underlying disease. Since the skin and nervous system are both ectodermal in origin, many hereditary and cong

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30

Skin in Psychoanalysis. Karnac Books, 2007.

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31

Skin in Psychoanalysis. Karnac Books, 2007.

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32

Skin in psychoanalysis. Karnac, 2007.

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33

Ulnik, Jorge. Skin in Psychoanalysis. Taylor & Francis Group, 2020.

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34

Ulnik, Jorge. Skin in Psychoanalysis. Taylor & Francis Group, 2019.

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35

Skin in Psychoanalysis. Karnac Books, 2007.

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36

Wolf, David S. Neurofibromatosis Type 1. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0051.

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Neurofibromatosis type 1 is a common, autosomal dominant, monogenetic neurocutaneous disorder. It is characterized by café au lait spots, axillary and inguinal freckling, Lisch nodules, optic pathway gliomas, neurofibromas, and distinctive bony abnormalities. Also associated with this condition are other central nervous system tumors, scoliosis, hypertension, vascular abnormalities, and cognitive issues such as learning disabilities and attention deficit-hyperactivity disorder.

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37

Gipson, Tanjala T., Andrea Poretti, Rebecca McClellan, and Michael V. Johnston. Tuberous Sclerosis Complex. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0050.

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Tuberous sclerosis complex (TSC) is a disease, commonly classified as a neurocutaneous disorder, which may result in benign tumors throughout the brain and body, skin lesions, epilepsy, and cognitive/behavioral difficulties. Scientific discovery in TSC has resulted in the availability of treatments designed to target the neurobiological core of TSC in children. However, research is needed to determine if these treatments are effective for multiple aspects of the TSC phenotype in children. Current pediatric research studies have focused on the effects of early treatment of epilepsy as well as i

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