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12 Possible Causes for Absent Pulp Chambers, Brachycephaly

  • Smith-Magenis Syndrome

    In addition, secondary teeth, particularly premolars, might be absent while the other teeth might display enlarged pulp chambers and reduced roots (taurodauntism).[symptoma.com] The common clinical findings were: speech delay with behavioural problems associated with broad flat midface, brachycephaly, broad nasal bridge and brachydactyly.[ncbi.nlm.nih.gov] Clinical manifestations include brachycephaly and a flat mid-face; brachydactyly; short, broad hands; mental retardation; and aberrant behaviour, including hyperactivity.[ncbi.nlm.nih.gov]

  • Autosomal Dominant Prognathism

    (short stature) oral manifestation: large pulp chambers, large pulp horns, cracks in dentin all the way to DEJ that may allow bacteria to get in and cause pulpal infections[quizlet.com] Patients have a distinctive facial appearance which includes low-set ears, brachycephaly, hypertelorism, exophthalmos, and mandibular prognathism.[icd10data.com] […] cleft palate, retroglossia, micrognathia, flat nasal bridge, malformed ears TF Twist TWIST 7p21 601622 Saethre-Chotzen syndrome 101400 AD craniosynostosis, acrocephaly, brachycephaly[en.wikibooks.org]

  • Dentinogenesis Imperfecta Type 1

    […] root canals Absent root tooth Amber colored teeth Misaligned teeth Recurring dental abscess Blue sclera Enamel separation from the ivory Very small pulp chambers Very small[medicalsubstance.com] Symptoms INHERITANCE: Autosomal recessive GROWTH: [Height]; Short stature (childhood); Birth length normal; [Weight]; Birth weight normal HEAD AND NECK: [Head]; Brachycephaly[findzebra.com] Symptoms of Dentinogenesis imperfecta Type I It is characterized by several tooth structure abnormalities, some of which include: Bluish-gray teeth Bulbous teeth crowns Absent[medicalsubstance.com]

  • X-Linked Mandibulofacial Dysostosis

    chambers, Pulp obliteration occurs after eruption, Roots of permanent and primary teeth are normal shape and length, Permanent teeth - pulp chambers are abnormally large,[quizlet.com] ; Brachycephaly; scaphocephaly; trigonocephaly; “cloverleaf” skull (kleeblattschädel) scaphocephaly; trigonocephaly; cloverleaf” (kleeblattschädel) Ocular proptosis: blindness[slideshare.net] […] cleft palate, retroglossia, micrognathia, flat nasal bridge, malformed ears TF Twist TWIST 7p21 601622 Saethre-Chotzen syndrome 101400 AD craniosynostosis, acrocephaly, brachycephaly[widesmiles2.org]

  • SHORT Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] A syndrome characterized by growth retardation, severe mental retardation, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth,[icd10data.com] […] skin that covers the inner eye (epicanthus folds) White flecks in the colored part of the eyes (Brushfield spots) Small ears A small head that's somewhat flat in the back (brachycephaly[verywellhealth.com]

  • Singleton Merten Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] Anotia Autoimmune neutropenia Flat face Vasculitis in the skin Cortical myoclonus Unilateral narrow palpebral fissure Midface retrusion Dilatation Agenesis of corpus callosum Brachycephaly[mendelian.co] […] recurvatum Expanded phalanges with widened medullary cavities Cardiac arrest Expanded metatarsals with widened medullary cavities Obesity Synophrys Irritability Anxiety Autism Brachycephaly[mendelian.co]

  • Hypophosphatasia

    Odontohypophosphatasia (AR or AD) Bone: loss of alveolar bone Dental: exfoliation (incisors) reduced dentin thickness enlarged pulp chambers caries AD: autosomal dominant[ada.org] Some affected babies later exhibit early fusion of the bones of the skull (craniosynostosis), which can result in the head appearing disproportionately wide (brachycephaly[rarediseases.org] Findings include undermineralized bones, widened-appearing sutures, brachycephaly, flail chest, rachitic costochondral rib changes (see Figure 1A ), flared metaphyses (resulting[ncbi.nlm.nih.gov]

  • Premature Tooth Eruption

    However, dental radiographs will indicate the enamel and pulp chamber changes already mentioned.[pocketdentistry.com] […] boring pain【穿孔痛】 *borreliosis【ボレリア感染症 ボレリア症】 lyme borreliosis【ライム*ボレリア感染症 ライム*ボレリア症】 *bovine tuberculosis【牛型結核(症)】 *bow elbow【内反肘】(cubitus varus) *bowen's disease【ボーエン病】 *brachycephaly[medo.jp] In addition, changes in the trabeculation of the alveolar bone along with abnormal or absent lamina dura can be observed radiographically [ 3 ].[pocketdentistry.com]

  • Taurodontia Absent Teeth Sparse Hair

    * Broad alveolar ridge * Thin nails * Large tooth pulp chambers Causes - Taurodontia absent teeth sparse hair Not supplied.[checkorphan.org] Feeding difficulties in infancy Fatigue Umbilical hernia Leukocytosis Infantile onset Dementia Dysarthria Splenomegaly Hernia Bronchiectasis Aplasia of the sweat glands Brachycephaly[mendelian.co] Radiographs show the extent of the invagination chamber. Enamel, which may be extremely thin or even absent, can be seen lining this chamber.[pocketdentistry.com]

  • Spondyloepimetaphyseal Dysplasia - Abnormal Dentition

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] […] with it often have. [10] Patient usually presents with a painless swelling in the area of the clavicles at 2 to 3 years of age. [11] Common features include: Head and neck: Brachycephaly[wikidoc.org] […] hypoplasia Small pituitary gland Rhizomelia Increased susceptibility to fractures Elevated alkaline phosphatase Coxa vara Abnormality of the skin Seizures Failure to thrive Brachycephaly[mendelian.co]

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