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1,709 Possible Causes for Absent Pulp Chambers, Allelic to Dentin Dysplasia Type 2, Craniosynostosis

  • 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] Pediatric Bone: Biology and Diseases, Glorieux et al, 2003 3. osteoporosis-pseudoglioma syndrome : severe form of OI that also causes blindness Cole-Carpenter syndrome : OI with craniosynostosis[radiopaedia.org] […] features that include congenital joint contractures and bone fragility [ 17 ] Cole-Carpenter syndrome - This is a severe progressive form of OI, with associated multisutural craniosynostosis[emedicine.staging.medscape.com]

  • Hypophosphatasia

    Craniosynostosis is accompanied by putatively functional consequences.[ncbi.nlm.nih.gov] Odontohypophosphatasia (AR or AD) Bone: loss of alveolar bone Dental: exfoliation (incisors) reduced dentin thickness enlarged pulp chambers caries AD: autosomal dominant[ada.org] Patients with HPP have defective bone mineralization as well as craniosynostosis that can be seen in the infantile and childhood forms of this disease.[ncbi.nlm.nih.gov]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Smith-Magenis Syndrome

    Gorlin, Craniosynostosis update 1987, American Journal of Medical Genetics, 31, S4, (99-148), (2005).[doi.org] In addition, secondary teeth, particularly premolars, might be absent while the other teeth might display enlarged pulp chambers and reduced roots (taurodauntism).[symptoma.com]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Autosomal Dominant Prognathism

    Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported.[orpha.net] (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] Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic acrocephaly, flat facies, high narrow palate Pfeiffer syndrome 101600 AD mild craniosynostosis, flat facies[en.wikibooks.org]

    Missing: Allelic to Dentin Dysplasia Type 2
  • Crouzon Syndrome

    Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca] Craniosynostosis: genes and mechanisms.[ncbi.nlm.nih.gov] Craniosynostosis. Eur J Hum Genet. 2011 Apr. 19 (4):369-76. [Medline]. [Full Text]. Ko JM. Genetic Syndromes Associated with Craniosynostosis.[emedicine.com]

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

    For this same photo without the arrows, click here For more information, click on the link if you see this icon Pediatric craniosynostosis. eMedicine.[learningradiology.com] A boy with brachycephaly without craniosynostosis, raised intracranial pressure, deafness, cataracts, and global developmental delay is described.[ncbi.nlm.nih.gov] Brachycephaly is a type of craniosynostosis.[symptoma.com]

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

    We present the first reported case associating MPS-I (Hurler-Scheie subtype) with craniosynostosis. A 2.5-year-old girl presented initially with macrocrania.[ncbi.nlm.nih.gov] […] syndrome with variable manifestations exhibiting mainly microcephaly, characteristic facies, mental retardation, short stature, acral skeletal anomalies with occasional craniosynostosis[icd9data.com]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • Mandibulofacial Dysostosis

    In conclusion, in children with syndromic or complex craniosynostosis, diagnosing OSA using home cardiorespiratory monitoring is feasible.[doi.org] Apert syndrome (Medical Encyclopedia) Cleidocranial dysostosis (Medical Encyclopedia) Craniosynostosis (Medical Encyclopedia) Craniosynostosis repair (Medical Encyclopedia[icdlist.com] Congenital craniofacial differences are conditions affecting the head and face that present at or shortly after birth such as craniosynostosis, cleft lip and palate, hemifacial[eng.ichacha.net]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2
  • Saethre-Chotzen Syndrome

    Furthermore, craniosynostosis was not present at birth or at the age of 4 months.[ncbi.nlm.nih.gov] Abstract Craniosynostosis or premature closure of the cranial sutures is a common abnormality occurring in about 1 in 2500 children.[ncbi.nlm.nih.gov] Craniosynostosis can happen before the baby is born or during the first few months of life.[sickkids.ca]

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

    […] sagittal craniosynostosis lambdoid sutures craniosynostosis pilonidal dimple absent coccyx spina bifida occulta scoliosis coxa v alga decreased hip-joint mobility flared[humpath.com] […] acrocephalopolysyndactyly (s) ( noun ), acrocephalopolysyndactylies (pl) Any of four heritable malformation syndromes recognizable at birth and characterized by premature craniosynostosis[wordinfo.info] From More Specific Terms Carpenter syndrome (acrocephalopolysyndactyly type 2) Pfeiffer's syndrome (acrocephalopolysyndactyly type 1) Introduction craniosynostosis syndromes[anvita.info]

    Missing: Absent Pulp Chambers Allelic to Dentin Dysplasia Type 2

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