CLEIDOCRANIAL DYSPLASIA (CCD) : A CASE REPORT
Journal Title: INTERNATIONAL JOURNAL OF ADVANCES IN ORTHOPAEDICS - Year 2018, Vol 1, Issue 3
Abstract
Cleidocranial dysplasia (CCD), also known as Scheuthauer Marie-Sainton Syndrome, is a rare autosomal dominant inherited disorder, characterized by general retardation in bone ossication, hypoplastic clavicles and various craniofacial and dental abnormalities. Early diagnosis of CCD can be difcult, because the majority of craniofacial abnormalities become obvious only during adolescence. CASE REPORT: In this case report, we describe an otherwise healthy 16 year-old male presented with hyper mobile shoulder, dental malformation and radiologically widening of sutures & presence of wormian bones, poorly formed sinuses & abnormal dentition, agenesis of mid portion of right clavicle with pseudo-arthrosis formation cone-shaped thorax, absence of pubic rami and narrow iliac wings hypoplastic and tapered distal phalanges of hand and spondylolysis at L3. CONCLUSION: Cleidocranial dysplasia is very rare in occurrence, incidence being 1: 1,000,000. Since early diagnosis of cleidocranial dysplasia is essential for initiating the appropriate treatment approach, clinicians should be aware of the characteristic features. We report a case of cleidocranial dysplasia because of its rarity
Authors and Affiliations
Dr. Sharat Balemane, Dr. S. tulasiram Yashaswi
Keywords
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