Case Of Cleidocranial Dysplasia Research Articles

A Case of Cleidocranial Dysplasia with Historical and Current Review

Introduction: This article discusses about our case of cleidocranial dysplasia and a review for dental manifestation and management of these cases. This disorder has a genetic background and general manifestations of CCD are outlined and an overview is presented. History: CCD is one of the best studies and documented disease whose history dates back to the prehistoric times with first case documented by Greig in 1933 in the museum of royal college of surgeons in Edinburgh. In the year of 1871, Scheuthauer published cranial and non – cranial findings of CCD. Case Report: We present a case of a 17 year old male patient who reported to our hospital with a complain of smaller and yellowish discolored teeth with spacing in the arch causing difficulty in chewing food. We have documented this case to the best of our understanding and with pictures depicting the patient and his clinical and radiographic findings. An interesting overview of the patient has been described. Discussion: We have researched different articles related to our patient and have documented the prominent features seen in these patients and correlated with the findings in our patient. There are reports of multiple patients who were diagnosed at a much earlier stage than our patient. Most of the clinical features described in the previous literature coincide with other findings, however additional clinical findings have been mentioned irrespective of their presence in our patient or not. Conclusion: We conclude that a proper clinical and radiographic evaluation can lead to early diagnosis of these patients and hence can aid in their management and education of the patient and his care takers. There are no reported cases of deficient IQ or abnormal life experienced by these patients except for that related to short stature.

Surgical treatment of multiple impacted supernumerary teeth in a cleidocranial dysplasia patient

AbstractTo report a case of cleidocranial dysplasia (CCD) with 15 supernumerary teeth and review the relevant literature. Diagnose and treat a CCD patient with 15 impacted supernumerary teeth in the maxilla and mandible. When CCD is accompanied by supernumerary teeth ambushed in the jaw and does not affect the health of the body, it can be regarded as a part of normal bone tissue. If X‐ray or computed tomography examination shows that supernumerary teeth affect permanent tooth eruption, the replacement process of adjacent teeth and permanent tooth eruption should be closely observed, and supernumerary teeth should be extracted in time if necessary.

Cleidocranial dysplasia: A rare case report

Cleidocranial dysplasia (CD) is a rare autosomal dominant skeletal disorder, characterised by typical oral and skeletal disorders, the most striking feature of which is malformation or absence of clavicles, open anterior frontanelle, presence of wormian bones and multiple dental abnormalities such as delayed exfoliation / eruption or supernumerary teeth. Mostly such patients are first noticed by the dentist due to aesthetic reasons or delayed eruption eruption of teeth. In this paper, a case of CD in a 16 year old female is reported and the literature is reviewed.

Cleidocranial Dysplasia: A Case Report

Cleidocranial Dysplasia is a disorder of teeth, jaws and other bones of body which arise.>due to chromosomal abnormalities, (autosomal dominant disorder). A case of cleidocranial dysplasia is presented who had classical diagnostic features of the syndrome

Classic case of cleidocranial dysplasia with an infected mandibular cyst

Classic case of cleidocranial dysplasia with an infected mandibular cyst

Anesthetic management of a case of cleidocranial dysplasia

Hereby, we present the case of an adult with cleidocranial dysplasia who underwent multiple tooth extraction. In this article, characteristics of this genetic disorder and implications for an anesthesiologist are being discussed.

Aesthetic Facial Correction of Cleidocranial Dysplasia.

We report two cases of cleidocranial dysplasia, which was managed without significant craniofacial osteotomy. A mother and daughter, both of normal intelligence, presented with central forehead depression, mid-face hypoplasia, and blepharoptosis. The fact that they have an identically deformed face implied a genetic basis. In both patients, radiologic evaluation revealed the underdeveloped maxilla, persistent fontanelle opening, and cleidal aplasia. Clinical findings and radiologic studies were consistent with the diagnosis of cleidocranial dysplasia. Both patients underwent forehead plasty via bicoronal approach, augmentation rhinoplasty using tip plasty, and epicanthoplasty. In addition, the mother underwent malar augmentation using Medpor implantation and reduction genioplasty. The patients did not experience any postoperative complication and remained satisfied with the operation at 6-year follow-up.

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

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.

Multiple Supernumerary Teeth Associated with Bony Malformations

Full blown cases of cleidocranial dysplasia (CCD) have been reported earlier but a case with a rarity of 60 teeth associated with bony malformations, is seldom observed Because of the oral findings this condition has been diagnosed at an early age, thus helping to achieve a better oral harmony. This article reports an atypical case with 16 supernumerary teeth associated with bony malformations.

Cleidocranial dysplasia: A case report

Summary Cleidocranial dysplasia (CCD) is a very rare congenital malformation syndrome that has an extremely varied presentation. This condition not only affects the membranous bones (e.g., clavicles, skull, flat bones) but it also affects endochondral ossification, leading to a generalized disorder of the skeletal structures. Despite its global skeletal manifestations, CCD tends to cause the greatest abnormalities within the skull, spine and dentition of the individuals affected. This article reports on a rare case of cleidocranial dysplasia in an otherwise healthy 18-year-old female.

Cleidocranial dysplasia with bilateral polycystic ovarian disease and Mullerian abnormality of the uterus: a case report

We report an interesting case of cleidocranial dysplasia associated with an unusual finding of bilateral polycystic ovarian disease and bicornuate uterus with unicollis (Mullerian abnormality).

Cleidocranial dysplasia in a mother and her daughter within the scope of neurosurgery

Cleidocranial dysplasia is an autosomal-dominant disorder characterized by late closure or nonclosure of the anterior fontanelle, late ossification of cranial sutures, defective clavicle, and delayed eruption of permanent teeth. In this article, two cases of cleidocranial dysplasia involving a mother and her daughter are reported, and a case management policy is suggested. The 1-year-old daughter was macrocephalic and brachycephalic, and had midface hypoplasia and hypertelorism. Plain radiographs revealed aplasia of the clavicles. Three-dimensional computerized tomography scanning demonstrated a large anterior fontanelle, a patent posterior fontanelle, and bone defects at the pterion and asterion, together with nonfused metopic and sagittal sutures. The mother was 22 years of age. She had an open anterior fontanelle, aplastic clavicles, and unerupted permanent teeth. Although it is a rare disorder, cleidocranial dysplasia should be recognized by neurosurgeons. A protective helmet can be provided in early childhood, and craniofacial remodeling can be undertaken at a later age, when the final size and shape of the skull become apparent.