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Relevant bibliographies by topics / Cutis marmorata telangiectatica congenita

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Academic literature on the topic 'Cutis marmorata telangiectatica congenita'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 April 2022

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Journal articles on the topic "Cutis marmorata telangiectatica congenita"

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Sharma, Jyoti. "Cutis marmorata telangiectatica congenita." Journal of Clinical Neonatology 2, no. 4 (2013): 199. http://dx.doi.org/10.4103/2249-4847.123107.

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Ponnurangam, VinothN, and Venkataraman Paramasivam. "Cutis marmorata telangiectatica congenita." Indian Dermatology Online Journal 5, no. 1 (2014): 80. http://dx.doi.org/10.4103/2229-5178.126042.

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Garzon, Maria C., and Eric Schweiger. "Cutis marmorata telangiectatica congenita." Seminars in Cutaneous Medicine and Surgery 23, no. 2 (June 2004): 99–106. http://dx.doi.org/10.1016/j.sder.2004.01.003.

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Manikoth, P. "Cutis marmorata telangiectatica congenita." Archives of Disease in Childhood - Fetal and Neonatal Edition 90, no. 2 (March 1, 2005): F169. http://dx.doi.org/10.1136/adc.2004.064303.

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KENNEDY, CORNELIS, ARNOLD P. ORANJE, KOOS KEIZER, MARY M. HEUVEL, and CORIENE E. CATSMAN-BERREVOETS. "CUTIS MARMORATA TELANGIECTATICA CONGENITA." International Journal of Dermatology 31, no. 4 (April 1992): 249–52. http://dx.doi.org/10.1111/j.1365-4362.1992.tb03564.x.

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Khambati, Nisreen, Jacob Reading, Sian Osborn, Danielle Bucke, and Atanu Dutta. "Cutis marmorata telangiectatica congenita." Archives of Disease in Childhood - Fetal and Neonatal Edition 106, no. 1 (July 6, 2020): 75. http://dx.doi.org/10.1136/archdischild-2020-319612.

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Georgesco, Gabriella, and Gérard Lorette. "Cutis marmorata telangiectatica congenita." La Presse Médicale 39, no. 4 (April 2010): 495–98. http://dx.doi.org/10.1016/j.lpm.2009.09.026.

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Broeckx, W., M. Ledoux-Corbusier, and J. Delescluse. "Cutis marmorata congenita telangiectatica." Dermatology 176, no. 3 (1988): 154–56. http://dx.doi.org/10.1159/000248695.

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Cheever, Eileen. "Cutis Marmorata Telangiectatica Congenita." Physician Assistant Clinics 1, no. 2 (April 2016): 265–75. http://dx.doi.org/10.1016/j.cpha.2015.12.004.

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Hafsi, W., N. El Fekih, N. Ezzine, S. Kamoun, M. Bani, and B. Fazaa. "Cutis marmorata telangiectatica congenita." Annales de Dermatologie et de Vénéréologie 140 (April 2013): S45. http://dx.doi.org/10.1016/j.annder.2013.01.020.

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Dissertations / Theses on the topic "Cutis marmorata telangiectatica congenita"

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CAHUZAC, PARADIS ISABELLE. "Le cutis marmorata telangiectatica congenita : a propos de 6 cas." Montpellier 1, 1991. http://www.theses.fr/1991MON11105.

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HOFMANN, CARRETERO SOPHIE. "Cutis marmorata telangiectatica congenita : a propos de 10 cas et revue de la litterature." Toulouse 3, 1993. http://www.theses.fr/1993TOU31500.

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Révolte, Michèle. "Phacomatose pigmentovasculaire type IIIb : association inédite à une schizophrénie, une cutis marmorata telangiectatica congenita et à des collagénomes éruptifs : à propos d'un cas, revue de la littérature." Montpellier 1, 1991. http://www.theses.fr/1991MON11080.

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GOMARD, PHILIPPE. "Le syndrome d'adams-oliver : a propos d'un cas." Reims, 1992. http://www.theses.fr/1992REIMM066.

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Dias, Ana Sofia dos Santos. "Cutis marmorata: uma revisão da literatura." Master's thesis, 2020. http://hdl.handle.net/10316/97877.

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Trabalho Final do Mestrado Integrado em Medicina apresentado à Faculdade de Medicina
A Cutis Marmorata (CM) consiste num reticulado eritemato-cianótico que dá à pele um aspeto marmoreado. Possui duas variantes, a CM fisiológica e a Cutis Marmorata Telangiectática Congénita (CMTC). Existem diferenças importantes entre as duas formas da CM que ajudam no diagnóstico diferencial. A CM fisiológica surge nos recém-nascidos (RN) e é uma alteração cutânea benigna e transitória que não tem nenhum significado patológico. É um achado dermatológico extremamente comum na idade pediátrica. Resulta de uma resposta vasomotora exagerada ao frio por imaturidade do sistema nervoso autónomo, e geralmente desaparece com a aplicação de calor local. A CMTC constitui uma malformação capilar rara, de aspecto clínico característico e etiologia desconhecida. Pode estar presente ao nascimento ou surgir nos primeiros dias de vida. Na pele são visíveis telangiectasias, localizadas ou generalizadas, associadas a um eritema reticular, e tem tipicamente uma distribuição segmentar. O seu diagnóstico é clínico. Apesar de ser descrita como uma condição benigna, pode apresentar atrofia e ulcerações cutâneas, bem como outras malformações associadas, como o glaucoma congénito e assimetria corporal. O diagnóstico diferencial é um desafio dado que muitas entidades apresentam características clínicas que podem mimetizar a CMTC. Geralmente não é necessário qualquer tratamento, uma vez que a maioria das lesões cutâneas acaba por melhorar ou regredir com o tempo, mas é importante monitorizar regularmente estes pacientes durante a infância.
Cutis marmorata (CM) is an erythematous-cyanotic reticulate that gives the skin a marbled appearance. It has two variants, physiological CM and Cutis Marmorata Telangiectatica Congenita (CMTC). Important differences exist between the two variants that can help in the differential diagnosis. Physiological CM appears in newborns and is a benign transient cutaneous lesion that has no pathological meaning. It’s an extremely common dermatological finding in small children. It results from an exaggerated vasomotor response to cold due to immaturity of the autonomic nervous system and usually disappears with local warming. CMTC is a rare capillary malformation, with characteristic clinical findings and unknown etiology. It can be present at birth or appear in the first days of the newborn's life. Localized or generalized telangiectasias are visible on the skin, associated with a reticular erythema, and these lesions typically present with a segmental distribution. Diagnosis is made on clinical grounds. It´s usually described as a benign disorder but cutaneous atrophy and ulcerations may be present, as well as other associated malformations, such as congenital glaucoma and body asymmetry. The differential diagnosis can present challenges, given that many conditions have clinical manifestations that can mimic CMTC. Usually doesn’t require treatment, as most cutaneous lesions tend to fade over time, but is important to maintain a regular monitorization of these patients during infancy.

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Books on the topic "Cutis marmorata telangiectatica congenita"

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Sybert, Virginia P. Disorders of the Dermis. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0005.

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Collagen – Ainhum – Amniotic Bands – Buschke-Ollendorff Syndrome – Dermatosparaxis – Ehlers-Danlos Syndromes – Ehlers-Danlos Types I, II, and III – Ehlers-Danlos Type IV – Ehlers-Danlos Type VI – Ehlers-Danlos Type VIII – Reactive Perforating Collagenosis – Elastin – Costello Syndrome – Cutis Laxa – Pseudoxanthoma Elasticum – Vascular – Ataxia Telangiectasia – Blue Rubber Bleb Nevus Syndrome – Cutis Marmorata Telangiectatica Congenita – Fabry Syndrome – Familial Flame Nevi – Hereditary Glomus Tumors – Hereditary Hemorrhagic Telangiectasia – Klippel-Trenaunay-Weber Syndrome – Maffucci Syndrome – Sturge-Weber Syndrome – Mixed – Aplasia Cutis Congenita – Focal Dermal Hypoplasia – Tuberous Sclerosis – Other Disorders of the Dermis – Albright Hereditary Osteodystrophy – Cutis Verticis Gyrata – Familial Dysautonomia – François Syndrome – Lipoid Proteinosis – Multiple Pterygia – Systemic Hyalinosis

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Sybert, Virginia P. Disorders of the Dermis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0005.

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Chapter 5 covers Collagen disorders (Ainhum, Amniotic Bands, Buschke-Ollendorff Syndrome, Dermatosparaxis), Ehlers-Danlos Syndromes (Ehlers-Danlos Types I, II, and III, Ehlers-Danlos Type IV, Ehlers-Danlos Type VI, Ehlers-Danlos Type VIII, and Reactive Perforating Collagenosis), Elastin (Costello Syndrome, Cutis Laxa, and Pseudoxanthoma Elasticum), Vascular disorders (Ataxia Telangiectasia, Cutis Marmorata Telangiectatica Congenita, Fabry Syndrome, Familial Flame Nevi, Hereditary Glomus Tumors, Hereditary Hemorrhagic Telangiectasia, Klippel-Trenaunay-Weber Syndrome, Maffucci Syndrome, and Sturge-Weber Syndrome, and Multiple Cutaneous and Mucosal Venous Malformations), Mixed disorders (Aplasia Cutis Congenita, Focal Dermal Hypoplasia, Tuberous Sclerosis Complex), and other Disorders of the Dermis (Albright Hereditary Osteodystrophy, Cutis Verticis Gyrata, Familial Dysautonomia, François Syndrome, Hyaline Fibromatosis Syndrome, Lipoid Proteinosis, and Multiple Pterygia). Each condition is discussed in detail, including dermatologic features, associated anomalies, histopathology, basic defect, treatment, mode of inheritance, prenatal diagnosis, and differential diagnosis.

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Book chapters on the topic "Cutis marmorata telangiectatica congenita"

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Peters, Nils, Martin Dichgans, Sankar Surendran, Josep M. Argilés, Francisco J. López-Soriano, Sílvia Busquets, Klaus Dittmann, et al. "Cutis Marmorata Telangiectatica Congenita." In Encyclopedia of Molecular Mechanisms of Disease, 479–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-29676-8_3138.

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Chen, Harold. "Cutis Marmorata Telangiectatica Congenita." In Atlas of Genetic Diagnosis and Counseling, 705–13. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-2401-1_62.

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Chen, Harold. "Cutis Marmorata Telangiectatica Congenita." In Atlas of Genetic Diagnosis and Counseling, 1–8. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6430-3_62-2.

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Panteliadis, Christos P. "Cutis Marmorata Telangiectatica Congenita (Van Lohuizen’s Syndrome)." In Neurocutaneous Disorders, 209–13. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-87893-1_15.

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Lapunzina, Pablo, and Jill Clayton-Smith. "Macrocephaly-Cutis Marmorata Telangiectatica Congenita (Macrocephaly-Capillary Malformation)." In Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes, 323–32. Vienna: Springer Vienna, 2008. http://dx.doi.org/10.1007/978-3-211-69500-5_12.

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Varga, Rita, Ilana Goldscheider, Sarah Basedow, Kathrin Giehl, and Peter Kaudewitz. "Cutis marmorata teleangiectatica congenita." In Fortschritte der praktischen Dermatologie und Venerologie 2012, 607–10. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-24767-5_84.

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Pfützner, Wolfgang, Christian A. Sander, and Gerd Plewig. "Retracted Chapter: Cutis marmorata teleangiectatica congenita." In Fortschritte der praktischen Dermatologie und Venerologie, 676. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55661-6_119.

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Mancini, Anthony J., and Daniel P. Krowchuk. "Cutis marmorata telangiectatica congenita." In Dermatologie de L'enfant, 334–37. Elsevier, 2019. http://dx.doi.org/10.1016/b978-2-294-75852-2.00054-7.

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"Cutis Marmorata Telangiectatica Congenita." In Atlas of Genetic Diagnosis and Counseling, 537–43. New York, NY: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-1037-9_62.

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"Cutis marmorata telangiectatica congenita." In Pediatric Dermatology and Dermatopathology, 79–80. CRC Press, 2001. http://dx.doi.org/10.1201/b14322-30.

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Conference papers on the topic "Cutis marmorata telangiectatica congenita"

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Hamed, Amel Ben, Afef Ben Thabet, Chiraz Regaieg, Manel Charfi, Ridha Regaieg, Nedia Hmida, Abderahmen Masmoudi, Hamida Turki, Amira Bouraoui, and Abdellatif Gargouri. "P589 Cutis marmorata telangiectatica congenita." In Faculty of Paediatrics of the Royal College of Physicians of Ireland, 9th Europaediatrics Congress, 13–15 June, Dublin, Ireland 2019. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2019. http://dx.doi.org/10.1136/archdischild-2019-epa.923.

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