Case Report
BibTex RIS Cite

Cranial MRI findings in a case with Seckel syndrome

Year 2018, , 312 - 314, 30.09.2018
https://doi.org/10.7197/223.vi.417787

Abstract

Özet



 



Seckel sendromu (SS) nadir,
heterojen bir primordiyal cücelik türüdür. Zeka geriliği ve nörolojik
belirtilerin varlığı bu sendromun kendine has özelliklerinden biridir. Biz
burada Seckel sendromlu bir çocuk hastada kraniyal MR bulgularını sunuyoruz.



 



Abstract



 



Seckel’s syndrome (SS) is a rare,
heterogeneous form of primordial dwarfism. The presence of mental retardation
and neurologic signs is one of the peculiar features of this syndrome. We
herein present the cranial MR findings in a child patient with Seckel's
syndrome.

References

  • Reference 1 Shanske A, Caride DG, Menasse-Palmer L, Bogdanow A, Marion RW. Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature. Am J Med Genet. 1997; 70: 155–8.
  • Reference 2 Kutlu R, Alkan A, Kutlu O, Yakinci C. Seckel syndrome with polyarteritis nodosa. Indian Pediatr 2004; 41: 1158-61.
  • Reference 3 Arnold SR, Spicer D, Kouseff B et al. Seckel-Like Syndrome in Three Siblings. Pediatr Dev Pathol. 1999; 2: 180–7.
  • Reference 4 Howanietz H, Frisch H, Jedlicka-Kobler I, Stegar H. Seckel Dwarfism based on a Personal Observation. Klin Pediatr. 1989; 201: 139–41.
  • Reference 5 Cherian MP. Seckel-like syndrome or Seckel variants? Ann Saudi Med 2004; 24: 469–72.
  • Reference 6 Krishna AG, Scrimgeour EM, Zawawi TH. Seckel Syndrome in a Yemeni Family in Saudi Arabia. Am J Med Genet 1994; 51: 224–7.
  • Reference 7 Sugio Y, Tsukahara M, Kajii T. Two Japanese cases with microcephalic primordial dwarfism: classical Seckel syndrome and osteodysplastic primordial dwarfism type II. Jpn J Hum Gene Genet 1993; 38: 209–17.
  • Reference 8 D'Angelo VA, Ceddia AM, Zelante L, Florio FP. Multiple intracranial aneurysms in a patient with Seckel syndrome. Childs Nerv Syst. 1998; 14: 82 -4.
  • Reference 9 Can F, Ovalı Yılmaz G, Özkol M, Tarhan S. Seckel Sendromunda Görüntüleme Bulguları. Turkiye Klinikleri J Pediatr 2009;18: 328-31.
Year 2018, , 312 - 314, 30.09.2018
https://doi.org/10.7197/223.vi.417787

Abstract

References

  • Reference 1 Shanske A, Caride DG, Menasse-Palmer L, Bogdanow A, Marion RW. Central nervous system anomalies in Seckel syndrome: report of a new family and review of the literature. Am J Med Genet. 1997; 70: 155–8.
  • Reference 2 Kutlu R, Alkan A, Kutlu O, Yakinci C. Seckel syndrome with polyarteritis nodosa. Indian Pediatr 2004; 41: 1158-61.
  • Reference 3 Arnold SR, Spicer D, Kouseff B et al. Seckel-Like Syndrome in Three Siblings. Pediatr Dev Pathol. 1999; 2: 180–7.
  • Reference 4 Howanietz H, Frisch H, Jedlicka-Kobler I, Stegar H. Seckel Dwarfism based on a Personal Observation. Klin Pediatr. 1989; 201: 139–41.
  • Reference 5 Cherian MP. Seckel-like syndrome or Seckel variants? Ann Saudi Med 2004; 24: 469–72.
  • Reference 6 Krishna AG, Scrimgeour EM, Zawawi TH. Seckel Syndrome in a Yemeni Family in Saudi Arabia. Am J Med Genet 1994; 51: 224–7.
  • Reference 7 Sugio Y, Tsukahara M, Kajii T. Two Japanese cases with microcephalic primordial dwarfism: classical Seckel syndrome and osteodysplastic primordial dwarfism type II. Jpn J Hum Gene Genet 1993; 38: 209–17.
  • Reference 8 D'Angelo VA, Ceddia AM, Zelante L, Florio FP. Multiple intracranial aneurysms in a patient with Seckel syndrome. Childs Nerv Syst. 1998; 14: 82 -4.
  • Reference 9 Can F, Ovalı Yılmaz G, Özkol M, Tarhan S. Seckel Sendromunda Görüntüleme Bulguları. Turkiye Klinikleri J Pediatr 2009;18: 328-31.
There are 9 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Case Reports
Authors

Mehmet Atalar

Publication Date September 30, 2018
Acceptance Date July 10, 2018
Published in Issue Year 2018

Cite

AMA Atalar M. Cranial MRI findings in a case with Seckel syndrome. CMJ. September 2018;40(3):312-314. doi:10.7197/223.vi.417787