A RARE CASE OF SHPRINTZEN-GOLDBERG SYNDROME

Authors

  • Parvathy Chitran Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India
  • Sreela L.S Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India
  • Philips Mathew Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India
  • Twinkle S Prasad Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India

Abstract

Shprintzen-Goldberg syndrome is a relatively rare congenital connective tissue type of disorder with a constellation of dysmorphic features including craniosynostosis, craniofacial, skeletal, cardiovascular and neurological abnormalities. We present the case-report of a 5-year-old boy with Shprintzen-Goldberg syndrome and a brief review of literature pertaining to this condition. The patients with Shprintzen-Goldberg syndrome show a considerable phenotypic overlap with other craniosynostosis syndromes. So, a meticulous evaluation of these patients should be performed for a prudent diagnosis. Since these patients present with multiple systemic conditions,a multidisciplinary approach should be planned for their management.

Keywords: Brachycephaly; Cleftpalate; Craniosynostosis; Cryptorchidism; Hypertelorism; Uvula

Author Biographies

Parvathy Chitran, Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India

JUNIOR RESIDENT

ORAL MEDICINE AND RADIOLOGY

Sreela L.S, Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India

PROFESSOR AND HEAD OF THE DEPARTMENT,

ORAL MEDICINE AND RADIOLOGY

Philips Mathew, Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India

ASSISTANT  PROFESSOR 

ORAL MEDICINE AND RADIOLOGY

Twinkle S Prasad, Department of Oral Medicine and Radiology, KUHS university, Government Dental College Kottayam-India

ASSOCIATE  PROFESSOR 

ORAL MEDICINE AND RADIOLOGY

References

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Greally MT, Carey JC, Milewicz DM, Hudgins L, Goldberg RB, Shprintzen RJ, et al. Shprintzen-Goldberg syndrome: a clinical analysis. Am J Med Genet 1998;76(3):202-12.

Pauliks LB, Chan KC, Lorts A, Elias ER, Cayre RO, Valdes-Cruz LM. Shprintzen-Goldberg Syndrome with Tetralogy of Fallot and Subvalvar Aortic Stenosis. J Ultrasound Med 2005;24(5):703-6.

Pavone V, Leonardi R, Sorge G, Pavone P, Pratico A, Sessa G. Apatient with Shprintzen Goldberg syndrome. Clinical follow-up for twelve years. J Pediatr Sci 2012;4(4):1-6.

Kosaki K, Takahashi D, Udaka T, Kosaki R, Matsumoto M, Ibe S, et al. Molecular pathology of Shprintzen-Goldberg syndrome. Am J Med Genet A 2006;140(1):104-8.

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Published

2021-02-21

How to Cite

Chitran, P., L.S, S., Mathew, P., & Prasad, T. S. (2021). A RARE CASE OF SHPRINTZEN-GOLDBERG SYNDROME. Journal of Ayub Medical College Abbottabad, 33(1), 155–158. Retrieved from https://jamc.ayubmed.edu.pk/index.php/jamc/article/view/7611