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Ellis-van Creveld Sendromu (Kondroektodermal Displazi) Bir Olgunun Sunumu: Tek Atrium ve Persistan Sol Süperior Vena Kava Birlikteliği

Year 2013, Volume: 7 Issue: 2, 89 - 93, 01.08.2013

Abstract

Ellis-van Creveld (EvC) sendromu, otosomal resesif olarak kalıtılan nadir bir kondral ve ektodermal hastalıktır. Kondro ve ektodermal displazi, polidaktili ve konjenital kalp defektleri bu sendromun karakteristik bulgularıdır. Tek atrium ve endokardiyal yastık defektlerinin bu sendromda en sık rastlanan konjenital kalp defektleri olduğu bildirilmektedir. EvC sendromunun nadir görülmesi nedeni ile ekokardiyografik ve anjiyokardiyografik incelemede, tek atrium ve persistan sol süperior vena kava gibi doğumsal kalp anomalilerinin yanı sıra EvC sendromunun diğer klasik bulguları saptanan dört yaşındaki kız hasta sunulmuştur.

References

  • Ellis RW, van Crefeld S. A syndrome characterized by ectodermaldysplasia, congenital morbus cardia. Arch Dis Child 1940;15:65.
  • Shilpy S, Nikhil M, Samir D. Ellis van Creveld syndrome. J Indian Soc Pedod Prev Dent 2007;25:5-7.
  • Baujat G, Le Merrer M. Ellis-van Creveld syndrome. Orphanet J Rare Dis 2007; 27:1-5.
  • Venkat-Raman N, Sebire NJ, Murphy KM, Carvalho JS, Hall CM. Increased first-trimester fetal nuchal translucent thickness in association with chondroectodermal dysplasia (Ellis-Van Creveld Syndrome). Ultrasound Obstet Gynecol 2005;25:412-14.
  • Polymeropoulos MH, Ide SE, Wright M, Goodship J, Weissenbach J, Pyeritz RE, et al. The gene for the Ellis-van Creveld syndromes located on choromosome 4p16. Genomics 1996;35:1-5.
  • Varela M, Ramos C. Chondroectodermal dysplasia (Ellis-van Creveld syndrome): A case report. Eur J Orthod 1996;18:313-18.
  • Kamesui T, Seki M, Tsubota M, Endo M, Watanabe S, Sato H. A case of Ellis-van Creveld syndrome with partial atrioventricular septal defect and double orifice mitral valve. Nippon Kyobu Geka Gakkai Zasshi 1997;45:589-93.
  • Santos JM, Pipa J, Antunes L, Neves O, Nascimento C, Cabral C, et. al. The Ellis-Van Creveld syndrome. Apropos 2 clinical cases. Rev Port Cardiol 1994;13:45-50.
  • Chang YC, Wu JM, Lin SJ, Wu MH. Common atrium with Ebstein’s anomaly in a neonate with Ellis-van Creveld syndrome. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1995;36:50-2.
  • Lacro RV. Dysmorphology and Genetics. In: Keane JF, Lock JE, Fyler DC (eds). NADA’s Pediatric Cardiology. 2nd ed. Philadelphia: Saunders Elsevier, 2006:68.
  • Lucas RV, Krabil KA. Abnormal systemic venous connections. In: Emmanouilides GC, Riemenschneider TA, Allen HD, Gutgesell HP (eds). Heart Disease in İnfants, Children, and Adolescents Including the Fetus and Young Adult. 5th ed. Volume 1. Baltimore: Williams & Wilkins, 1995:875-78.
  • Bhat YJ, Baba AN, Manzoor S, Qayoom S, Javed S, Ajaz H. Ellis- van Creveld syndrome with facial hemiatrophy. Indian J Dermatol Venerol Leprol 2010;76:266-69.
  • Pirazzoli P, Mazzanti L, Mandini M, Cau M, Ravagli L, Cacciari E. GH deficiency in Ellis-van-Creveld Syndrome: Response to replacement theraphy. Growth Abnormalities 1989;56:391-94.
  • Elçioğlu NH, Hall CM. Diagnostic dilemmas in the short rib-polydactyly syndrome group. Am J Med Genet 2002;111:392- 400.

Ellis-van Creveld Syndrome (Chondroectodermal Dysplasia) A Case Report: Association of Common Atrium and Persistent Left Superior Vena Cava

Year 2013, Volume: 7 Issue: 2, 89 - 93, 01.08.2013

Abstract

The Ellis-van Creveld (EvC) syndrome (EvC) is a rare chondral and ectodermal dysplasia inherited autosomal recessively. The EvC syndrome is characterized by chondrodysplasia and ectodermal dysplasia, polydactyly, and congenital cardiac defects. It is reported that common atrium and endocardial cushion defects are the most common congenital cardiac defects in patients with the EvC syndrome. Here, a four-year-old girl with the diagnostic features of EvC syndrome and a common atrium with persistent left superior vena cava demonstrated by echocardiographic and angiocardiographic investigations is described because of the rarity of this syndrome

References

  • Ellis RW, van Crefeld S. A syndrome characterized by ectodermaldysplasia, congenital morbus cardia. Arch Dis Child 1940;15:65.
  • Shilpy S, Nikhil M, Samir D. Ellis van Creveld syndrome. J Indian Soc Pedod Prev Dent 2007;25:5-7.
  • Baujat G, Le Merrer M. Ellis-van Creveld syndrome. Orphanet J Rare Dis 2007; 27:1-5.
  • Venkat-Raman N, Sebire NJ, Murphy KM, Carvalho JS, Hall CM. Increased first-trimester fetal nuchal translucent thickness in association with chondroectodermal dysplasia (Ellis-Van Creveld Syndrome). Ultrasound Obstet Gynecol 2005;25:412-14.
  • Polymeropoulos MH, Ide SE, Wright M, Goodship J, Weissenbach J, Pyeritz RE, et al. The gene for the Ellis-van Creveld syndromes located on choromosome 4p16. Genomics 1996;35:1-5.
  • Varela M, Ramos C. Chondroectodermal dysplasia (Ellis-van Creveld syndrome): A case report. Eur J Orthod 1996;18:313-18.
  • Kamesui T, Seki M, Tsubota M, Endo M, Watanabe S, Sato H. A case of Ellis-van Creveld syndrome with partial atrioventricular septal defect and double orifice mitral valve. Nippon Kyobu Geka Gakkai Zasshi 1997;45:589-93.
  • Santos JM, Pipa J, Antunes L, Neves O, Nascimento C, Cabral C, et. al. The Ellis-Van Creveld syndrome. Apropos 2 clinical cases. Rev Port Cardiol 1994;13:45-50.
  • Chang YC, Wu JM, Lin SJ, Wu MH. Common atrium with Ebstein’s anomaly in a neonate with Ellis-van Creveld syndrome. Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi 1995;36:50-2.
  • Lacro RV. Dysmorphology and Genetics. In: Keane JF, Lock JE, Fyler DC (eds). NADA’s Pediatric Cardiology. 2nd ed. Philadelphia: Saunders Elsevier, 2006:68.
  • Lucas RV, Krabil KA. Abnormal systemic venous connections. In: Emmanouilides GC, Riemenschneider TA, Allen HD, Gutgesell HP (eds). Heart Disease in İnfants, Children, and Adolescents Including the Fetus and Young Adult. 5th ed. Volume 1. Baltimore: Williams & Wilkins, 1995:875-78.
  • Bhat YJ, Baba AN, Manzoor S, Qayoom S, Javed S, Ajaz H. Ellis- van Creveld syndrome with facial hemiatrophy. Indian J Dermatol Venerol Leprol 2010;76:266-69.
  • Pirazzoli P, Mazzanti L, Mandini M, Cau M, Ravagli L, Cacciari E. GH deficiency in Ellis-van-Creveld Syndrome: Response to replacement theraphy. Growth Abnormalities 1989;56:391-94.
  • Elçioğlu NH, Hall CM. Diagnostic dilemmas in the short rib-polydactyly syndrome group. Am J Med Genet 2002;111:392- 400.
There are 14 citations in total.

Details

Other ID JA86ZP86HH
Journal Section Research Article
Authors

Hayrullah Alp This is me

Fatih Şap This is me

Hakan Altın This is me

Zehra Karataş This is me

Tamer Baysal This is me

Sevim Karaaslan This is me

Publication Date August 1, 2013
Submission Date August 1, 2013
Published in Issue Year 2013 Volume: 7 Issue: 2

Cite

Vancouver Alp H, Şap F, Altın H, Karataş Z, Baysal T, Karaaslan S. Ellis-van Creveld Syndrome (Chondroectodermal Dysplasia) A Case Report: Association of Common Atrium and Persistent Left Superior Vena Cava. Türkiye Çocuk Hast Derg. 2013;7(2):89-93.


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