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A case of Asphyxiated Thoracic Dystrophy (Jeune Syndrome) diagnosed in neonatal period

Year 2020, Volume: 17 Issue: 3, 465 - 467, 30.09.2020
https://doi.org/10.38136/jgon.665794

Abstract



Jeune Syndrome is a rare
autosomal recessive inherited skeletal chondrodystrophy. Patients usually die
of respiratory failure during early infancy. The disease has a wide clinical pi
cture including renal dysplasia, hepatic and pancreatic fibrosis. Here,
we present a case of Jeune Syndrome diagnosed by narrowing of thoracic anterior
posterior and transverse diameter and flattening of acetabular ceiling. We
aimed to emphasize the necessity of early diagnosis and close monitoring
because of the risk of sudden death.

References

  • 1. Vries J. de, Yntema J.L. , Van die C.E , Crama N. ,Cornelissen E.A.M , Hamel B.C.J , Jeune syndrome: description of 13 cases and a proposal for follow-up protocol. Eur J Pediatr, 2010. 169(1): p. 77-88.
  • 2. Turkel, S.B., Diehl E.J. and Richmond J.A. , Necropsy findings in neonatal asphyxiating thoracic dystrophy. J Med Genet, 1985. 22(2): p. 112-8.
  • 3. Waters, A.M. and P.L. Beales, Ciliopathies: an expanding disease spectrum. Pediatr Nephrol, 2011. 26(7): p. 1039-56.
  • 4. CHRISTINE A. GLEASON, S.E.J., Avery's Diseases of the Newborn, 2018. TENTH EDİTİON(jeune syndrome): p. 1257.
  • 5. Casamassima M.G.S. ,Goldstein S.D., Salazar J.H., Papandria D., Mclltrot K., Abdullah F. et al, Operative management of acquired Jeune's syndrome. Journal of Pediatric Surgery, 2014. 49(1): p. 55-60.
  • 6. Digoy, G.P., M. Greenberg, and A. Magit, Congenital stridor secondary to an upper airway cyst in a patient with Ellis-van Creveld syndrome. Int J Pediatr Otorhinolaryngol, 2005. 69(10): p. 1433-5.
  • 7. Patel, S.H., Banzali F.M Jr., Post R.J., Nguyen C.V., Benoit R.M., Tieu D.D., et al., Parturient With Barnes Syndrome (Thoracolaryngopelvic Dysplasia) Undergoing Cesarean Delivery of a Neonate With Barnes Syndrome: A Case Report. A A Pract, 2018. 11(6): p. 151-154.
  • 8. Balci, S., Altinok G., Tekşen F., Eryilmaz M., A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts. Turk J Pediatr, 2003. 45(2): p. 174-8.

Yenidoğan döneminde tanı alan Asfiktik Torasik Distrofi (Jeune Sendromu) vakası

Year 2020, Volume: 17 Issue: 3, 465 - 467, 30.09.2020
https://doi.org/10.38136/jgon.665794

Abstract

Jeune Sendromu nadir görülen otozomal resesif kalıtım gösteren bir iskelet kondrodistrofisidir. Hastalar genellikle solunum yetmezliğinden erken süt çocukluğu döneminde kaybedilirler. Hastalık renal displazi, hepatik ve pankreatik fibrozisi içeren geniş bir klinik tabloya sahiptir. Burada toraks ön arka ve transvers çapta daralma, asetabular tavanda düzleşme saptanarak tanı konulan Jeune Sendromlu bir olguyu sunduk. Ani ölüm riski taşımaları nedeniyle erken tanınıp yakından takip edilebilmesi gerekliliğini vurgulamayı amaçladık.

References

  • 1. Vries J. de, Yntema J.L. , Van die C.E , Crama N. ,Cornelissen E.A.M , Hamel B.C.J , Jeune syndrome: description of 13 cases and a proposal for follow-up protocol. Eur J Pediatr, 2010. 169(1): p. 77-88.
  • 2. Turkel, S.B., Diehl E.J. and Richmond J.A. , Necropsy findings in neonatal asphyxiating thoracic dystrophy. J Med Genet, 1985. 22(2): p. 112-8.
  • 3. Waters, A.M. and P.L. Beales, Ciliopathies: an expanding disease spectrum. Pediatr Nephrol, 2011. 26(7): p. 1039-56.
  • 4. CHRISTINE A. GLEASON, S.E.J., Avery's Diseases of the Newborn, 2018. TENTH EDİTİON(jeune syndrome): p. 1257.
  • 5. Casamassima M.G.S. ,Goldstein S.D., Salazar J.H., Papandria D., Mclltrot K., Abdullah F. et al, Operative management of acquired Jeune's syndrome. Journal of Pediatric Surgery, 2014. 49(1): p. 55-60.
  • 6. Digoy, G.P., M. Greenberg, and A. Magit, Congenital stridor secondary to an upper airway cyst in a patient with Ellis-van Creveld syndrome. Int J Pediatr Otorhinolaryngol, 2005. 69(10): p. 1433-5.
  • 7. Patel, S.H., Banzali F.M Jr., Post R.J., Nguyen C.V., Benoit R.M., Tieu D.D., et al., Parturient With Barnes Syndrome (Thoracolaryngopelvic Dysplasia) Undergoing Cesarean Delivery of a Neonate With Barnes Syndrome: A Case Report. A A Pract, 2018. 11(6): p. 151-154.
  • 8. Balci, S., Altinok G., Tekşen F., Eryilmaz M., A 34-week-old male fetus with short rib polydactyly syndrome (SRPS) type I (Saldino-Noonan) with pancreatic cysts. Turk J Pediatr, 2003. 45(2): p. 174-8.
There are 8 citations in total.

Details

Primary Language Turkish
Subjects Paediatrics
Journal Section Case Reports
Authors

Fevzi Kahveci 0000-0002-5176-1040

Evrim Alyamac Dizdar 0000-0001-8956-0917

Fatma Sarı 0000-0003-4643-7622

Publication Date September 30, 2020
Submission Date December 27, 2019
Acceptance Date April 22, 2020
Published in Issue Year 2020 Volume: 17 Issue: 3

Cite

Vancouver Kahveci F, Alyamac Dizdar E, Sarı F. Yenidoğan döneminde tanı alan Asfiktik Torasik Distrofi (Jeune Sendromu) vakası. JGON. 2020;17(3):465-7.