Relevant bibliographies by topics / Amniotic Band Syndrome

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Academic literature on the topic 'Amniotic Band Syndrome'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Amniotic Band Syndrome"

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Kostyukov, Kostyukov K. V. "Amniotic band syndrome." Akusherstvo i ginekologiia 10_2020 (October 20, 2020): 204–9. http://dx.doi.org/10.18565/aig.2020.10.204-209.

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Cherian, Vigy Elizebth. "Amniotic Band Syndrome." International Journal of Nursing Education and Research 7, no. 4 (2019): 605. http://dx.doi.org/10.5958/2454-2660.2019.00135.2.

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Kumar, M., S. Das, and B. Kumar. "Amniotic Band Syndrome." Ultrasound 15, no. 2 (May 2007): 96–98. http://dx.doi.org/10.1179/174313407x192549.

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Ray, Mark, Sophia J. Hendrick, Sharon S. Raimer, and Steven J. Blackwell. "Amniotic Band Syndrome." International Journal of Dermatology 27, no. 5 (June 1988): 312–14. http://dx.doi.org/10.1111/j.1365-4362.1988.tb02359.x.

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Obritsch, Jerry M., and Michael S. Cardwell. "AMNIOTIC BAND SYNDROME." Southern Medical Journal 83, Supplement (September 1990): 2S—38. http://dx.doi.org/10.1097/00007611-199009001-00145.

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PANT, R., HARIQBAL SINGH, and G. NARULA. "AMNIOTIC BAND SYNDROME." Medical Journal Armed Forces India 57, no. 2 (April 2001): 172–73. http://dx.doi.org/10.1016/s0377-1237(01)80148-9.

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Walter, John H., Larry R. Goss, and Alicia T. Lazzara. "Amniotic band syndrome." Journal of Foot and Ankle Surgery 37, no. 4 (July 1998): 325–33. http://dx.doi.org/10.1016/s1067-2516(98)80070-7.

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Turner, Barbara S. "Amniotic Band Syndrome." Journal of Obstetric, Gynecologic & Neonatal Nursing 14, no. 4 (July 1985): 298–301. http://dx.doi.org/10.1111/j.1552-6909.1985.tb02243.x.

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Idris, UmmaAbdullahi. "Amniotic band syndrome." Archives of Medicine and Health Sciences 6, no. 2 (2018): 260. http://dx.doi.org/10.4103/amhs.amhs_24_17.

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Richardson, Sonya McFerrin, Kathy Gill, and Larry Arcement. "Amniotic Band Syndrome." Journal of Diagnostic Medical Sonography 10, no. 3 (May 1994): 137–43. http://dx.doi.org/10.1177/875647939401000302.

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Books on the topic "Amniotic Band Syndrome"

1

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 "Amniotic Band Syndrome"

1

Abdel-Rehim, Shady, and Kevin Chung. "Amniotic Band Syndrome." In Congenital Anomalies of the Upper Extremity, 295–303. Boston, MA: Springer US, 2014. http://dx.doi.org/10.1007/978-1-4899-7504-1_22.

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Sasor, Sarah E., and Kevin C. Chung. "Amniotic Band Syndrome." In Congenital Anomalies of the Upper Extremity, 395–405. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-64159-7_23.

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"Amniotic Band Syndrome." In Diagnostic Imaging: Musculoskeletal Non-Traumatic Disease, 691. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39252-5.50174-8.

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"Amniotic Band Syndrome." In Diagnostic Imaging: Obstetrics, 924–27. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-323-39256-3.50248-x.

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"Amniotic band syndrome." In Dermatology Therapy, 43–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_184.

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Clark, Robin D., and Cynthia J. Curry. "Lower Extremity Anomalies." In Genetic Consultations in the Newborn, edited by Robin D. Clark and Cynthia J. Curry, 211–16. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199990993.003.0031.

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This chapter reviews the incidence, epidemiology, genetics, and anatomical varieties of congenital anomalies of the lower extremity. Defects can be transverse, longitudinal, intercalary, or central and involve the femur, tibia, or fibula and there are combined defects and conditions affecting both upper and lower extremity. Isolated transverse defects are less common in the lower extremity than the upper but amniotic band disruption sequence can affect both upper and lower limbs. Adams Oliver syndrome affects both upper and lower limbs. Femoral facial syndrome is the most common lower extremity syndrome. Split hand/split foot is clinically heterogeneous and complex albeit with several well characterized syndromes including those caused by variants in TP63 and the 17p1.3. chromosome duplicaton syndrome . The clinical case presentation features an infant with fibular aplasia, tibial campomelia, and oligosyndactyly due to FATCO syndrome, a condition whose genetic cause is unknown.
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Clark, Robin D., and Cynthia J. Curry. "Upper Extremity Anomalies." In Genetic Consultations in the Newborn, edited by Robin D. Clark and Cynthia J. Curry, 203–10. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199990993.003.0030.

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This chapter reviews background information about the incidence, epidemiology, genetics, and other anomalies associated with common congenital anomalies of the upper extremity. The discussion reviews the differential diagnosis of transverse, longitudinal (amelia, radial, ulnar), intercalary (phocomelia), and central (split hand/foot) defects of the radius and ulna and combined upper and lower extremity defects. The chapter summarizes common causes of upper extremity anomalies, including amniotic band disruption sequence, teratogenic agents (misoprostol, thalidomide, valproic acid), vascular disruption, chromosome anomalies, and Mendelian congenital malformation syndromes, and it gives recommendations for evaluation and management. A clinical case presentation features an infant with Holt–Oram syndrome.
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"Fetoscopy and the Single Fetus: Diagnostic Embryofetoscopy, Bladder Obstruction, Amniotic Band Syndrome, and the Technological Fix." In Looking Within. The MIT Press, 2007. http://dx.doi.org/10.7551/mitpress/7383.003.0008.

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