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2,607 Possible Causes for Absent Pulp Chambers, Craniosynostosis, Low Set Ears

  • 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).[] Gorlin, Craniosynostosis update 1987, American Journal of Medical Genetics, 31, S4, (99-148), (2005).[] ears, and brachydactyly.[]

  • Mandibulofacial Dysostosis

    In conclusion, in children with syndromic or complex craniosynostosis, diagnosing OSA using home cardiorespiratory monitoring is feasible.[] An exam of the infant may reveal a variety of problems, including: Abnormal eye shape Flat cheekbones Cleft palate or lip Small jaw Low-set ears Abnormally formed ears Abnormal[] Apert syndrome (Medical Encyclopedia) Cleidocranial dysostosis (Medical Encyclopedia) Craniosynostosis (Medical Encyclopedia) Craniosynostosis repair (Medical Encyclopedia[]

    Missing: Absent Pulp Chambers
  • Down Syndrome

    Boyadjiev, Genetic advances in craniosynostosis, American Journal of Medical Genetics Part A, 173, 5, (1406-1429), (2017) ., Practice Bulletin No. 187, Obstetrics & Gynecology[] […] variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set[] […] syndrome there is a level of cognitive impairment, as well as the characteristic craniofacial features, such as an anteriorly and posteriorly flattened head, dysplastic low-set[]

    Missing: Absent Pulp Chambers
  • Rubinstein-Taybi Syndrome

    The term craniosynostosis refers to an abnormality in which the bones in an infant's skull fuse prematurely.[] Prominent and beaked nose, hypoplasia of the maxilla, low-set ears, micrognathia, enamel hypoplasia, talon cusps, highly arched eyebrows and long eyelashes are the most common[] […] syn·drome ( rū'bĭn-stīn tā'bē ), mental retardation, broad thumb and great toe, antimongoloid slant to the eyes, thin and beaked nose, microcephaly, prominent forehead, low-set[]

    Missing: Absent Pulp Chambers
  • Saethre-Chotzen Syndrome

    Furthermore, craniosynostosis was not present at birth or at the age of 4 months.[] Clinical features of this syndrome include unilateral or bilateral coronal synostosis, ptosis, low-set ears, hearing loss, hypertelorism, maxillary hypoplasia, deviated nasal[] The patient described in this report displayed craniofacial features classic for Saethre–Chotzen syndrome, including craniosynostosis, low-set ears, small pinna with prominent[]

    Missing: Absent Pulp Chambers
  • 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,[] Apert syndrome 101200 AD craniosynostosis, brachysphenocephalic acrocephaly, flat facies, high narrow palate Pfeiffer syndrome 101600 AD mild craniosynostosis, flat facies[] ears Low set ears Lowset ears [ more ] 0000369 Specific learning disability 0001328 X-linked inheritance 0001417 Showing of 29 Last updated: 5/1/2019 If you need medical[]

  • Hypophosphatasia

    Odontohypophosphatasia (AR or AD) Bone: loss of alveolar bone Dental: exfoliation (incisors) reduced dentin thickness enlarged pulp chambers caries AD: autosomal dominant[] Craniosynostosis is accompanied by putatively functional consequences.[] […] to thrive short, bowed extremities, generalised hypotonia, a small funnel chest, soft calvaria, very large fontanel, extremely wide cranial sutures, high-arched palate, low-set[]

  • 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[] Areas covered include: Craniosynostosis Syndromes; Syndromes Affecting Bone; Metabolic and Autoimmune Syndromes; Syndromes Affecting Skin and Mucosa; Hamartoneoplastic Syndromes[] Clinical features: flattened face with maxillary hypoplasia relative mandibular prognathism low set ears hypertelorism depressed nasal bridge high arched palate Short broad[]

  • Cerebellotrigeminal Dermal Dysplasia

    This boy was evaluated shortly after birth because of suspected craniosynostosis.[] Other features observed in patients were craniosynostosis, midfacial hypoplasia, bilateral corneal opacities, low-set ears, short stature, moderate intellectual impairment[] Diseases related with Low-set ears and Corneal opacity In the following list you will find some of the most common rare diseases related to Low-set ears and Corneal opacity[]

    Missing: Absent Pulp Chambers
  • Cloverleaf Skull

    Richard Hayward, Barry Jones, David Dunaway, Robert Evans Cambridge University Press, ٠٩‏/٠١‏/٢٠٠٤ - 421 من الصفحات Clinics in Developmental Medicine No. 163 Children with craniosynostosis[] Besides a trilobed skull and abnormalities of the extremities, he had low-set ears, stenosis of both external auditory canals, a beak-like nose, microphthalmia, retentio testis[] Craniosynostosis. Am Fam Physician. 2004 Jun 15;69(12):2863-2870. 3.0 3.1 3.2 3.3 Craniosynostosis and Craniofacial Disorders.[]

    Missing: Absent Pulp Chambers

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