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10 Possible Causes for Absent Pulp Chambers, Anemia

  • Hypophosphatasia

    Relatively few conditions are associated with a low serum alkaline phosphatase including Wilson's disease, hypophosphatasia, pernicious anemia and untreated hypothyroidism[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] Three clinical types are recognized: [1] infantile (symptoms beginning between birth and 6 months and characterized by severe softening of bones, fever, anemia, vomiting,[annals.org]

  • Uncinate Seizure

    […] tooth roots – canals – pulp chambers • Too small tooth roots – canals – pulp chambers • Enamel separation from the ivory (dentin) • Misaligned teeth – Recurring dental abscess[worlddentalnetwork.com] Syndrome,*Acquired immuneodeficiency syndrome (AIDS),Alcohol, Effects of,Alopecia,Alpers' (Disease),Alpha Rhythm ,AmbulatoryEEG,, Ammonia, *Ammon's horn,*Amnesia,Amygdala,Anemia[springerpub.com] […] mentioned in various sources for Dentinogenesis imperfecta, type I includes the 14 symptoms listed below: • Bluish-gray teeth – Amber-colored teeth – Bulbous teeth crowns • Absent[worlddentalnetwork.com]

  • Autosomal Dominant Prognathism

    […] and updated coverage, increased worldwide perspectives, and many new contributors keep you current on the late preterm infant, the fetal origins of adult disease, neonatal anemia[books.google.com] (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] Affected individuals may also experience rhinitis, hepatosplenomegaly, anemia and extramedullary hematopoiesis.[rarediseases.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] These may appear as anemia, hyperkeratosis (scaling of the skin), easy bruising, muscle spasms, poor blood clotting, and bone pain.[en.wikipedia.org] Problems associated with dehydration and malnutrition include weight loss, weakness, fatigue, anemia, and bacterial infections.[medicinenet.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] anemia (DBA) have been reported.[iths.pure.elsevier.com] COX4I2, C15orf41, KIF23, KLF1 Moderate to severe macrocytic anemia presenting occasionally in utero as severe anemia associated with hydrops fetalis but more commonly in[centogene.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] , Xeroderma pigmentosum FANCA Fanconi anemia FANCB Fanconi anemia FANCC Fanconi anemia FANCD2 Fanconi anemia FANCE Fanconi anemia FANCF Fanconia anemia FANCG Fanconi anemia[genda.com.ar] Key words Dental dysplasia aortic calcification anemia This is a preview of subscription content, log in to check access. Preview Unable to display preview.[link.springer.com]

  • Amelogenesis imperfecta Type 1C

    . shape and size of crown and root are relatively normal density, obliteration of pulp chamber presence of periapical radiolucency without pulpal involvement Gingival Health[de.slideshare.net] […] dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant sensory ataxia 1 autosomal dominant sideroblastic anemia[rgd.mcw.edu] […] dysplasia, Pakistani type spondyloepimetaphyseal dysplasia, Sponastrime type temtamy preaxial brachydactyly syndrome thalassemia thiamine-responsive megaloblastic anemia[rgd.mcw.edu]

  • Amelogenesis imperfecta Type Hypomaturation

    chambers in single rooted teeth and a bow tie appearance of the pulp chambers of permanent molars?[quizlet.com] 2 autosomal recessive pyridoxine-refractory sideroblastic anemia 3 autosomal recessive Robinow syndrome autosomal recessive type IV Ehlers-Danlos syndrome Bardet-Biedl syndrome[rgd.mcw.edu] About 1 month before the exam, he was submitted to iron treatment due to slight anemia. On examination, he was in good general health.[blackstar.forp.usp.br]

  • Taurodontism Microdontia and Dens Invaginatus

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] […] inerstitial fluid, mucosa, skin and developing teeth causes of hyperbilirubinemia -erythroblastosis fetalis -biliary atresia -premature birth -internal hemorrhage hemolytic anemia[quizlet.com] Thalassemia Thanatophoric dysplasia Glasgow variant Thanatophoric dysplasia type 1 Thanatophoric dysplasia type 2 Theodor Hertz Goodman syndrome Thiamine responsive megaloblastic anemia[personalizedcause.com]

  • Spondyloepimetaphyseal Dysplasia - Abnormal Dentition 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] Shprintzen Omphalocele Syndrome OMIM:260400 Shwachman-Diamond Syndrome 1; SDS1 OMIM:617941 Shwachman-Diamond Syndrome 2; SDS2 OMIM:269921 Sialuria OMIM:603903 Sickle Cell Anemia[informatics.jax.org] […] 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]

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