Create issue ticket

568 Possible Causes for Absent Pulp Chambers, Allelic to Dentin Dysplasia Type 2, Delayed Dentition

  • 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] dentition.[ncbi.nlm.nih.gov] […] facial features such as triangular facies, lack of facial fat, and hypoplastic nasal alae with overhanging columella, partial lipodystrophy, hernias, hyperextensibility, and delayed[uniprot.org]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Familial Hypophosphatemia

    chamber and numerous areas of interglobular dentine throughout the thickness of the dentine.[jisppd.com] Delayed dentition; dental abscesses; deafness; Chiari malformation; extraskeletal calcification of the tendons, ligaments, and joint capsules; and craniosynostosis are occasionally[emedicine.medscape.com] dentition, dental abscesses, and early tooth decay.[consultant360.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • 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 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]

    Missing: Delayed Dentition
  • Down Syndrome

    We report a case of chimpanzee trisomy 22 in a captive-born female. Because chromosome 22 in great apes is homologous to human chromosome 21, the present case is analogous to human trisomy 21, also called Down syndrome. The chimpanzee in the present case experienced retarded growth; infantile cataract and[…][ncbi.nlm.nih.gov]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • Facial Hemiatrophy

    - A dictionary of medical eponyms Related people Caleb Hillier Parry Moritz Heinrich Romberg A rare disorder characterized by progressive atrophy of some or all tissues on one side of the face, occasionally extending to other parts of the body. The process may be bilateral in 5% to 10% of cases. Tissues involved[…][whonamedit.com]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • Premature Tooth Eruption

    However, dental radiographs will indicate the enamel and pulp chamber changes already mentioned.[pocketdentistry.com] Keywords: Delayed dentitions, hypocalcemia, malnutrition, premature exfoliation of the tooth How to cite this article: Aliyu I.[mjdrdypu.org] If this delay goes beyond 6 months, talk to your dentist; Primary dentition will be completed between the second and third years of age, and some primary teeth will remain[orthodontisteenligne.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • 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] […] tooth-and-nail syndrome;tns;hypodontia-nail dysgenesis syndrome; tooth and nail syndrome; witkop syndrome Related symptoms: Autosomal dominant inheritance Abnormality of the dentition[mendelian.co] It is not reasonable for clinicians to delay treatment for those individuals exhibiting mandibular prognathism in an attempt to see the final phenotype, and conversely, could[studyres.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Vitamin D Deficiency

    dentition, delayed anterior fontanelle closure Investigations Infants Infants: Exclusively breastfed infants with at least one other risk factor without symptoms/signs -[rch.org.au] Previous vitamin D levels, previous/current treatments - to reduce risk of over-dosing Family understanding of Vitamin D Exam Signs of Rickets (deformity in growing bones) Delayed[rch.org.au]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • 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] […] the metacarpals, and dental anomalies including delayed eruption of permanent dentition and multiple supernumerary teeth.[ncbi.nlm.nih.gov] In addition, patients present with a delayed and defective mineralization of the dentition, together with a deficiency of acellular cementum.[raredr.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • 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] Intellectual disability Asthma Abnormality of the dentition Erythema High palate Growth delay Abnormal facial shape Seizures Ichthyosis Atrial septal defect Hyperkeratosis[mendelian.co] […] crown height, and the absent or small premolars in association with high frequency hearing loss. [20] Short Roots Associated with Short Stature but No Syndrome Generalized[indjos.com]

    Missing: Allelic to Dentin Dysplasia Type 2