Clinical spectrum of cleidocranial dysplasia: a case report
© Garg and Agrawal; licensee BioMed Central Ltd. 2008
Received: 11 November 2008
Accepted: 08 December 2008
Published: 08 December 2008
Cleidocranial dysplasia is a developmental anomaly of the skeleton and the teeth. This condition may be inherited, be transmitted as dominant characteristics in either sex, or even may appear spontaneously. It presents with skeletal defects of several bones, like partial or complete absence of clavicles, late closure of the fontanels, presence of open skull sutures and multiple wormian bones.
In this case report, we describe an otherwise healthy 30 year-old male with a chief complaint of missing anterior maxillary and Mandibular teeth.
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.
Cleidocranial dysplasia is a rare congenital defect of autosomal dominant inheritance, [1, 2] primarily affecting bones that undergo intra-membranous ossification, i.e. generally the calvarian but also the clavicular bones. It is also known as Marie and Sainton disease, Mutational dysostosis and Cleidocranial dysostosis . Cleidocranial dysplasia was first described by Pierre Marie and Paul Sainton in 1898,  since then, over 1000 cases have been documented in the medical literature .
Cleidocranial dysplasia presents with skeletal defects of several bones, the most striking of which are partial or complete absence of clavicles, late closure of the fontanels, presence of open skull sutures and multiple wormian bones [1, 6]. Late closure of fontanels is also a feature of Basal cell nevus syndrome and Crouzon syndrome, but together with other characteristic features, cleidocranial dysplasia can be easily differentially diagnosed. The skull base is dysplastic and reduced in growth resulting in increased skull width leading to brachycephaly and hypertelorism . Delayed closure of anterior fontanel and metopic sutures result in frontal bossing.
Thoracic cage is small and bell shaped with short ribs. Typically, clavicles are underdeveloped to varying degrees and in approximately 10 percent of cases, are completely absent. This allows excessive mobility of the shoulder girdle. Other bones may also be affected including long bones, the vertebral column, the pelvis and the bones of hands and feet .
Characteristically, patients with cleidocranial dysplasia, show prolonged retention of deciduous dentition and delayed eruption of permanent teeth. Adults with cleidocranial dysplasia have mixed dentition in their oral cavities. In addition, patients with this condition, frequently show a large number of unerupted supernumerary teeth, often mimicking a premolar. As many as 63 unerupted supernumerary teeth have been documented in one patient . Maxilla is also underdeveloped along with ill-formed paranasal sinuses. This condition is of clinical significance to every dentist due to the involvement of the facial bones, altered eruption patterns and multiple supernumerary teeth.
A 30 year-old male presented to Dental Surgery clinic, Jaipur, with a chief complaint of missing anterior teeth in upper and lower jaws. He told that he hadn't had any teeth in these regions of the jaws since childhood after his milk teeth shed away. Due to these missing teeth, he had an unpleasant smile that resulted in a psychological trauma to him while communicating with society members. He insisted for rehabilitation of his missing teeth and smile.
A diagnosis of cleidocranial dysplasia was confirmed and the patient was referred to prosthodontic department of Govt. Dental College & Hospital, Jaipur for prosthetic rehabilitation where he was given dentures for his missing teeth.
One of the most presumptive clinical findings of cleidocranial dysplasia is hypermobility of the shoulders . Due to partial or complete absence of the clavicles, the shoulders can be brought forward to close proximity to the chest. Bosselation is present owing to the failed closure of the metopic sutures and anterior fontanel . Hypertelorism  is a common finding and maxilla and paranasal sinuses present as being underdeveloped .
Dental findings are characterized by decreased eruptive force of both primary and permanent dentitions, prolonged retention of primary teeth  and increase in odontogenesis leading to excessive number of supernumerary teeth . There is a predisposition to develop numerous supernumerary teeth, particularly in mandibular premolar and maxillary anterior regions . Other than delayed, the permanent molars generally erupt without incident [1, 3]. Removal of primary or supernumerary teeth does not usually promote eruption of unerupted permanent teeth .
The radiographic evaluation of patients is the most important and reliable means to confirm the diagnosis, since radiological findings of cleidocranial dysplasia are pathognomonic, i.e. broad sutures, large fontanels persisting into adulthood, numerous wormian bones and numerous unerupted supernumerary teeth[1, 3].
Cervical or thoracic vertebral defects, supernumerary ribs, thoracic and lumber scoliosis, kyphosis or lordoisis, pelvic bony abnormalities and anomalies of phalangeal, tarsal, metatarsal, carpal and metacarpal bones are all systemic findings .
Fabrication of dentures over the unerupted teeth, and
Removal of teeth as they erupt, for very little bone structure would be left if supernumerary, impacted and unerupted teeth were all extracted at once.
The clinical findings of cleidocranial dysplasia, although present at birth, are often either missed or diagnosed at a much later time. Some cases are diagnosed through incidental findings by physicians, treating patients for unrelated conditions. Cleidocranial dysplasia may be identified by family history, excessive mobility of shoulders and radiographic pathognomonic findings of the chest, skull and jaws.
This is to be declared that a written informed consent was obtained from the patient for publication of this case report and accompanying images. A scanned copy of the consent is attached here.
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