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Larsen Syndrome

Yıl 2013, Cilt: 22 Sayı: 1, 80 - 85, 01.03.2013

Öz

Larsen syndrome is an inherited condition characterized by multiple joint dislocations and typical facial features including depressed nasal bridge with hypertelorism and a prominent forehead. There are only several cases reported since its first report by Larsen in 1950's. The aim of this review is to illustrate the pathogenesis, clinical features, diagnosis, and differential diagnosis of this condition.

Kaynakça

  • Gupta N, Kabra M. Larsen syndrome. Indian Pediatrics. 2008; 45:783-4.
  • Centre for Arab Genomic Studies. Larsen Syndrome, Autosomal Dominant. http://www.cags.org.ae/pdf/150250.pdf. (Accessed: Aug 2012)
  • Habermann ET, Sterling A, Dennis RI, Bronx. Larsen's syndrome: a heritable disorder. J Bone Joint Surg.1976; 58:558-61.
  • Orhan D, Balcı S, Deren O, Ütine EG, Başaran A, Kale G. Prenatally diagnosed lethal type Larsenlike syndrome associated with bifid tongue. Turk J Pediatrics. 2008; 50:395-9.
  • Kulkarni ML, Mohammed Z, Kulkarni PM. Larsen Syndrome- Lethal variety. Indian J Pediatr. 2005; 72:1053-4.
  • Kaya RA, Turkmenoglu O, Cavufioglu H, Dilbaz S, Aydin Y. Cervical pedicle screw fixation in a patient with larsen syndrome: a case report. Turkish Neurosurgery. 2006;16:48-52. Al-Kaissi A, Ammar C, Ghachema MB, Hammoub A, Chehidab FB. Facial features and skeletal abnormalities in Lars en syndrome: a study of three generations of a Tunisian family. Swiss Med Wkly. 2003; 133:625-8.
  • Perçin EF, Gedik R, Develioğlu H, Kunt T. Larsen's syndrome with dental anomalies: report of a case. ASDC J Dent Child. 2002; 69:172-4.
  • Tsang MC, Ling JY, King NM, Chow SK. Oral and craniofacial morphology of a patient with Larsen syndrome. J Craniofac Genet Dev Biol. 1986; 6:357-62.
  • Gorlin RJ, Cohen MM, Hennekam A. Syndromes of Head and Neck,4th Ed. New York, Oxford University Press, 2001.
  • Kulkarni ML, Basha MH, Hegade S, Kumarasamy TA, Kulkarni AM. Antenatal diagnosis of Larsen Syndrome. Indian J Pediatr. 2010; 77:819-20.

Larsen Sendromu

Yıl 2013, Cilt: 22 Sayı: 1, 80 - 85, 01.03.2013

Öz

Larsen sendromu çoğul eklem dislokasyonları, deprese burun köprüsü, hipertelorizm ve belirgin bir alın ile karakterize tipik yüz özellikleri olan bir kalıtsal durumdur. İlk olarak 1950'li yıllarda bildirilmiş olmasına karşın bildirilmiş olgu sayısı oldukça azdır. Bu yazının amacı, Larsen sendromunun patogenezi, klinik özellikleri, tanı ve ayırıcı tanısı hakkında bilgi vermektir.

Kaynakça

  • Gupta N, Kabra M. Larsen syndrome. Indian Pediatrics. 2008; 45:783-4.
  • Centre for Arab Genomic Studies. Larsen Syndrome, Autosomal Dominant. http://www.cags.org.ae/pdf/150250.pdf. (Accessed: Aug 2012)
  • Habermann ET, Sterling A, Dennis RI, Bronx. Larsen's syndrome: a heritable disorder. J Bone Joint Surg.1976; 58:558-61.
  • Orhan D, Balcı S, Deren O, Ütine EG, Başaran A, Kale G. Prenatally diagnosed lethal type Larsenlike syndrome associated with bifid tongue. Turk J Pediatrics. 2008; 50:395-9.
  • Kulkarni ML, Mohammed Z, Kulkarni PM. Larsen Syndrome- Lethal variety. Indian J Pediatr. 2005; 72:1053-4.
  • Kaya RA, Turkmenoglu O, Cavufioglu H, Dilbaz S, Aydin Y. Cervical pedicle screw fixation in a patient with larsen syndrome: a case report. Turkish Neurosurgery. 2006;16:48-52. Al-Kaissi A, Ammar C, Ghachema MB, Hammoub A, Chehidab FB. Facial features and skeletal abnormalities in Lars en syndrome: a study of three generations of a Tunisian family. Swiss Med Wkly. 2003; 133:625-8.
  • Perçin EF, Gedik R, Develioğlu H, Kunt T. Larsen's syndrome with dental anomalies: report of a case. ASDC J Dent Child. 2002; 69:172-4.
  • Tsang MC, Ling JY, King NM, Chow SK. Oral and craniofacial morphology of a patient with Larsen syndrome. J Craniofac Genet Dev Biol. 1986; 6:357-62.
  • Gorlin RJ, Cohen MM, Hennekam A. Syndromes of Head and Neck,4th Ed. New York, Oxford University Press, 2001.
  • Kulkarni ML, Basha MH, Hegade S, Kumarasamy TA, Kulkarni AM. Antenatal diagnosis of Larsen Syndrome. Indian J Pediatr. 2010; 77:819-20.
Toplam 10 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Derleme
Yazarlar

Ramachandran Sudarshan Bu kişi benim

Yayımlanma Tarihi 1 Mart 2013
Yayımlandığı Sayı Yıl 2013 Cilt: 22 Sayı: 1

Kaynak Göster

AMA Sudarshan R. Larsen Sendromu. aktd. Mart 2013;22(1):80-85.