Add like
Add dislike
Add to saved papers

Pyknodysostosis: Report of a Rare Case and its Dental Management.

Aim: This is a case report of a 16-year-old girl visiting MR Ambedkar Dental College and Hospital (Department of Pedodontics and Preventive Dentistry) for dental treatment.

Background: Osteopetrosis acroosteolytica or Toulouse-Lautrec syndrome or pyknodysostosis is a rare autosomal recessive bone dysplasia, characterized by osteosclerosis, and short stature. Montanari described a patient with an unusual variation of achondroplasia, which in retrospect was the first case of pyknodysostosis to be reported.1 .

Case description: A 16-year-old girl reported to the Department of Pediatric and Preventive Dentistry with a chief complaint of pain in the lower left back region of the jaw since past 2 weeks.

Conclusion: Pyknodysostosis is a rare condition that is diagnosed basically on its clinical and radiographic features.

Clinical significance: It is important to recognize these features so that correct diagnosis can be made. This allows the treatment and prevention of future complications and ensures a better quality of life to the patient.

How to cite this article: Jawa A, Setty JV, Vijayshankar LV, et al. Pyknodysostosis: Report of a Rare Case and its Dental Management. Int J Clin Pediatr Dent 2020;13(2):192-195.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app