Journal of the Anatomical Society of India

CASE REPORT
Year
: 2021  |  Volume : 70  |  Issue : 4  |  Page : 258--261

Osteosclerotic bone disorder - Pyknodysostosis


N Vinay Kumar1, TS Gugapriya2, Guru Thangiah Arun3 
1 Department of Anatomy, Government Medical College, Palakkad, Kerala, India
2 Department of Anatomy, All India Institute of Medical Sciences, Nagpur, Maharashtra, India
3 Department of Radiodiagnosis, SRM Trichy Medical College Hospital and Research Centre, Tiruchirappalli, Tamil Nadu, India

Correspondence Address:
Dr. N Vinay Kumar
Department of Anatomy, Government Medical College, NH.47, East Yakkara, Kunnathurmedu, Palakkad - 678 013, Kerala
India

Pyknodysostosis is an autosomal recessive osteoclastic dysfunction characterized by generalized hyperostosis and short stature which has mere 10 cases reported from India out of 133 globally reported cases. This rare disorder is due to defective lysosomal cysteine protease cathepsin K in chromosome 21. A male child of 11 years underwent radiological investigation for stunted growth. Examination revealed less height for age, retarded mandibular growth, dysmorphic facial growth, and proportionately short fingers. Radiological findings showed generalized osteosclorosis, hypoplastic paranasal air sinuses, spool-shaped dorsolumbar vertebral bodies, acro-osteolysis of terminal phalanges, and scalloped acetabulum with increased bone density. Management of child should be aimed at correcting anemia and primary prevention of fractures. The postnatal craniofacial development needs to be monitored. Long-term management should aim at genetic mapping and therapy with bone marrow transplantation.


How to cite this article:
Kumar N V, Gugapriya T S, Arun GT. Osteosclerotic bone disorder - Pyknodysostosis.J Anat Soc India 2021;70:258-261


How to cite this URL:
Kumar N V, Gugapriya T S, Arun GT. Osteosclerotic bone disorder - Pyknodysostosis. J Anat Soc India [serial online] 2021 [cited 2022 May 24 ];70:258-261
Available from: https://www.jasi.org.in/article.asp?issn=0003-2778;year=2021;volume=70;issue=4;spage=258;epage=261;aulast=Kumar;type=0