Cleidocranial dysplasia: A report of two cases

Mehta, Dhaval; Vachhani, Raj V.; Patel, Mayoor

doi:10.4103/0970-4388.85836

Cited by 12 publications

(9 citation statements)

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“…The typical bilateral absence of clavicles is only observed in 10% of cases of CCD; whereas hypoplastic acromial ends of the clavicle are more commonly seen,11 12 as was noticed in the present case. The widened pubic symphysis and sacroiliac joint, as was seen in this case, are due to delayed ossification.…”

Section: Discussionsupporting

confidence: 73%

Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient

et al. 2015

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Cleidocranial dysplasia (CCD), an autosomal dominant disorder with a prevalence of 1 in 1 000 000 individuals, presents with a wide range of variability. Dentists are often the first to encounter patients with CCD, some of whom do not show typical manifestations. Since it has similar features to other pathologies, CCD is misdiagnosed as other conditions. A 10-year-old boy suffering from CCD was misdiagnosed as having rickets and was referred for non-eruption of a few permanent teeth along with an unaesthetic facial appearance. Clinically and radiologically, a diagnosis of CCD was made. Currently, management of this patient's orofacial manifestations is underway.

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Section: Discussionsupporting

confidence: 73%

Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient

et al. 2015

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“…The permanent teeth generally lose their eruption stimulus and stay embedded, while the deciduous teeth are retained. Suggested factors for overretained deciduous teeth are lack of eruption potential and lack of cellular cementum on roots of permanent teeth, delayed mineralization of teeth, physical barrier-abnormal density of bone overlying the succedaneous teeth, and failure of bony crypt to resorb [13]. In our patient there was delayed eruption of permanent teeth and tooth buds of 32, 41, 42 were missing.…”

Section: Discussionmentioning

confidence: 85%

Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma

Chopra

Marwaha

Chaudhuri

et al. 2012

Case Reports in Dentistry

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Cleidocranial dysplasia is a rare autosomal disorder which manifests as partial or complete absence of clavicles, multiple supernumerary teeth, and delayed closure of fontanelle. Classical cases of cleidocranial dysplasia are easily diagnosed very early in the life. However, cases with partial manifestation of the syndrome and noncontributory family history are difficult to diagnose. Here, we report a case of 8.5-year-old girl child who presented with delayed tooth development (without any supernumerary teeth), anterior open fontanelle, and normal clavicles, thus resulting in a diagnostic dilemma.

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“…6). Complete clavicular agenesis is seen in 10% of patients, who have sloping and hypermobile shoulders [7], a small biacromial diameter, and the ability to approximate the shoulders anteriorly [8][9][10][11][12]. This hypermobility does not seem to promote instability of the glenohumeral joint, since reports of shoulder dislocation as a complication of CDD are scarce and always consist of anterior dislocation [12,13].…”

Section: Discussionmentioning

confidence: 98%

Cleidocranial dysplasia with bilateral posterior glenohumeral dislocation: A case-report

Hardy¹,

Thiong’o²,

Leroy³

et al. 2015

Orthopaedics & Traumatology: Surgery & Research

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A 31-year-old man experienced bilateral posterior glenohumeral dislocation during seizures. He had cleidocranial dysplasia with complete absence of both clavicles. Cleidocranial dysplasia is a rare inherited disease also known as Marie-Sainton syndrome and responsible for dental abnormalities well-known to stomatologists and dentists. Other manifestations include defective development of the skull bones and hypoplastic or aplastic clavicles. We found no previous reports of bilateral posterior glenohumeral dislocation in patients with cleidocranial dysplasia. The objective of this work was to look for an association between clavicular aplasia and posterior glenohumeral dislocation.

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Cleidocranial dysplasia: A report of two cases

Cited by 12 publications

References 0 publications

Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient

Cleidocranial dysplasia syndrome (CCD) with an unusual finding in a young patient

Hypodontia and Delayed Dentition as the Primary Manifestation of Cleidocranial Dysplasia Presenting with a Diagnostic Dilemma

Cleidocranial dysplasia with bilateral posterior glenohumeral dislocation: A case-report

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