Relevant bibliographies by topics / Hypomelanose ito

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters

Academic literature on the topic 'Hypomelanose ito'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Hypomelanose ito"

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Chavallier, C., S. Colon, G. Faraj, R. Bouvier, and P. Cochat. "P30 Glomerulopathie et hypomelanose de ito." Archives de Pédiatrie 2 (January 1995): S124. http://dx.doi.org/10.1016/0929-693x(95)90042-x.

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FUYUNO, Yoko, Makiko KIDO-NAKAHARA, and Masutaka FURUE. "Two Cases of Hypomelanosis of Ito." Nishi Nihon Hifuka 76, no. 1 (2014): 18–22. http://dx.doi.org/10.2336/nishinihonhifu.76.18.

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Bello-Germino, Daniella, Rasmey Chhin, Thu Tran, and Tetyana L. Vasylyeva. "Possible Correlation between Hypomelanosis of Ito and Wilms’ Tumor." Case Reports in Pediatrics 2018 (July 16, 2018): 1–4. http://dx.doi.org/10.1155/2018/5938120.

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Hypomelanosis of Ito is a neurocutaneous disorder characterized by skin manifestations in a characteristic pattern associated with musculoskeletal and central nervous system symptoms. Our patient was diagnosed with Wilms’ tumor stage I at age two and was also found to have distinct streaked areas of skin hyper- and hypopigmentation suggestive of Hypomelanosis of Ito. We believe that our patient’s clinical diagnoses of Hypomelanosis of Ito and Wilms’ tumor are interlinked. The connecting factor is yet to be identified. Our patient does not have a deletion of 11p13 associated with a defect in WT
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Millichap, J. Gordon. "Hypomelanosis of Ito." Pediatric Neurology Briefs 2, no. 7 (1988): 53. http://dx.doi.org/10.15844/pedneurbriefs-2-7-7.

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Sukumar, D., B. Nanda Kishore, CJ Chethan, and KT Ashique. "Hypomelanosis of ITO." Indian Journal of Dermatology 51, no. 1 (2006): 65. http://dx.doi.org/10.4103/0019-5154.25211.

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Sridhar, J., S. Narayan, and PLK Desylva. "Hypomelanosis of Ito." Medical Journal Armed Forces India 62, no. 1 (2006): 68–69. http://dx.doi.org/10.1016/s0377-1237(06)80163-2.

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Sybert, Virginia P. "Hypomelanosis of Ito." Pediatric Dermatology 7, no. 1 (1990): 74–76. http://dx.doi.org/10.1111/j.1525-1470.1990.tb01079.x.

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Reese, P. D., and G. F. Judisch. "Hypomelanosis of Ito." Archives of Ophthalmology 104, no. 8 (1986): 1136–37. http://dx.doi.org/10.1001/archopht.1986.01050200042038.

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Ardinger, Holly H. "Hypomelanosis of Ito." Archives of Neurology 43, no. 8 (1986): 848. http://dx.doi.org/10.1001/archneur.1986.00520080086032.

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Sullo, Federica, Agata Polizzi, Chiara Battaglini, et al. "Hypomelanosis of Ito." Journal of Pediatric Neurology 16, no. 05 (2018): 265–75. http://dx.doi.org/10.1055/s-0038-1667206.

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AbstractHypomelanosis of Ito (HI) is a congenital neurocutaneous syndrome presenting in the first year of life. It was first described by Ito in 1952 as a purely cutaneous disease presenting with skin hypopigmentation. Several extracutaneous manifestations were later described, and it is now known that several organs can be involved (including brain, muscle, bone, heart, eye, kidney, and teeth) and that the prognosis is strictly related to the number of involved organs. The incidence and prevalence of this syndrome have been estimated to range between 1 in 7,540 births and 1 in 82,000; the dis
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Dissertations / Theses on the topic "Hypomelanose ito"

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Chiesa, Sandra. "Hypomelanose de ito : a propos d'un cas avec revue de la litterature medicale : aspects cliniques et physiopathogeniques." Université Louis Pasteur (Strasbourg) (1971-2008), 1990. http://www.theses.fr/1990STR1M011.

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POSTIGO, PONS BRIGITTE. "Contribution a l'etude de la maladie de ito (ou incontinentia pigmenti achromians) : a propos d'une observation ; revue de la litterature." Toulouse 3, 1989. http://www.theses.fr/1989TOU31223.

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Le, Pelletier Beaufond Sylvie. "Hypomélanose de Ito : revue de littérature à propos d'un cas." Bordeaux 2, 1988. http://www.theses.fr/1988BOR25022.

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Sorlin, Arthur. "Caractérisation génomique des anomalies de la pigmentation cutanée en mosaïque." Thesis, Bourgogne Franche-Comté, 2019. http://www.theses.fr/2019UBFCI011.

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Introduction : Les dyschromies cutanées en mosaïque ont fait suspecter de longue date l’implication d’un mosaïcisme génétique sous-jacent. Ces évènements post-zygotiques sont cependant difficilement détectables par les techniques conventionnelles. Ainsi, les bases génétiques des dyschromies en mosaïque étaient restées mal connues. Matériel et méthodes : la cohorte M.U.S.T.A.R.D rassemble des échantillons d’ADN de biopsies cutanées de patients porteurs d’un mosaïcisme pigmentaire. Après une analyse phénotypique spécialisée, ces échantillons sont étudiés en séquençage à forte profondeur, d’exome
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Books on the topic "Hypomelanose ito"

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Sybert, Virginia P. Disorders of Pigmentation. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0004.

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Hyperpigmentation – Carney Complex – Dowling-Degos Disease – Dyskeratosis Congenita – Fanconi Anemia – Hemochromatosis – Incontinentia Pigmenti – LEOPARD Syndrome – Linear and Whorled Nevoid Hypermelanosis – McCune-Albright Syndrome – Naegeli Syndrome – Neurofibromatosis – Nevus Phakomatosis Pigmentovascularis – Peutz-Jeghers Syndrome – Universal Melanosis – Hypopigmentation – Albinisms – Albinism with Deafness – Hermansky-Pudlak Syndrome – Oculocutaneous Albinism Tyrosinase Negative – Oculocutaneous Albinism Tyrosinase Positive – Yellow Mutant Albinism – Cross Syndrome – Hypomelanosis of Ito
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Sybert, Virginia P. Disorders of Pigmentation. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0004.

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Chapter 4 covers Hyperpigmentation (including Carney Complex, Dowling-Degos Disease, Dyskeratosis Congenita, Fanconi Anemia, H Syndrome, Hemochromatosis, Incontinentia Pigmenti, LEOPARD Syndrome, Linear and Whorled Nevoid Hypermelanosis, McCune-Albright Syndrome, Naegeli Syndrome, Neurofibromatosis, Nevus Phakomatosis Pigmentovascularis, Peutz-Jeghers Syndrome, and Universal Melanosis) and Hypopigmentation ( Albinisms, Albinism with Deafness, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Tyrosinase Negative, Oculocutaneous Albinism Tyrosinase Positive, Yellow Mutant Albinism, Cross Syndro
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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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Book chapters on the topic "Hypomelanose ito"

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Chen, Harold. "Hypomelanosis of Ito." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-2401-1_128.

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Chen, Harold. "Hypomelanosis of Ito." In Atlas of Genetic Diagnosis and Counseling. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6430-3_128-2.

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Taibjee, Saleem M., and Celia Moss. "Hypomelanosis of Ito/Pigmentary Mosaicism." In Harper's Textbook of Pediatric Dermatology. Wiley-Blackwell, 2011. http://dx.doi.org/10.1002/9781444345384.ch131.

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Neynaber, Sven, and Jörg C. Prinz. "Retracted Chapter: Hypomelanosis Ito, Typ Blaschko." In Fortschritte der praktischen Dermatologie und Venerologie. Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/3-540-28691-8_139.

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Griebel, V., I. Krägeloh-Mann, M. Buchwald-Saal, M. Schöning, and R. Michaelis. "Drei Fälle von Hypomelanosis Ito mit Verlaufskontrolle." In Aktuelle Neuropädiatrie 1988. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74499-0_21.

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Pascual-Castroviejo, Ignacio, and Martino Ruggieri. "Hypomelanosis of Ito and Related Disorders (Pigmentary Mosaicism)." In Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes. Springer Vienna, 2008. http://dx.doi.org/10.1007/978-3-211-69500-5_16.

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Trawöger, R., U. Mayr, E. Steichen-Gersdorf, S. Felber, M. Sailer, and B. Haffner. "Hypomelanosis von Ito, assoziiert mit einem Plexuspapillom und einer X-autosomalen Translokation." In Aktuelle Neuropädiatrie 1990. Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-76833-0_67.

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Weissert, M., E. Boltshauser, E. Frenk, P. Bischoff, and A. Wehrli. "Hypomelanosis Ito — ein weniger bekanntes neurokutanes Syndrom: Beobachtungen bei 3 Patienten von 5, 20 und 31 Jahren." In Aktuelle Neuropädiatrie 1988. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74499-0_79.

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9

Perlman, S. L. "Hypomelanosis of Ito." In Encyclopedia of the Neurological Sciences. Elsevier, 2014. http://dx.doi.org/10.1016/b978-0-12-385157-4.01195-7.

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PASCUAL-CASTROVEIJO, IGNACIO. "Hypomelanosis of Ito." In Neurocutaneous Diseases. Elsevier, 1987. http://dx.doi.org/10.1016/b978-0-409-90018-7.50012-8.

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You might also be interested in the extended bibliographies on the topic 'Hypomelanose ito' for particular source types:
Journal articles
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