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1,867 Possible Causes for Absent Pulp Chambers, Delayed Dentition, Low Set Ears

  • Down Syndrome

    […] 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[] Some common physical signs of the disorder include a small head, flattened face, short neck, up-slanted eyes, low-set ears, enlarged tongue and lips, and sloping underchin[]

    Missing: Absent Pulp Chambers
  • SHORT Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[] set ears, small teeth, and small nose).[] dentition.[]

  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    Unlike those with other forms of Long QT syndrome, those with Andersen–Tawil syndrome often have characteristic physical features including low-set ears and a small lower[] Dental anomalies have also been reported including delayed loss of primary or ‘baby’ teeth (persistent primary dentition), multiple missing teeth (oligodontia), and teeth[] QT interval with a variety of ventricular arrhythmias (leading to predisposition to sudden cardiac death) and characteristic physical features: short stature, scoliosis, low-set[]

    Missing: Absent Pulp Chambers
  • Rubinstein-Taybi Syndrome

    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[] […] descent of testes and hypospadias in males Dental Problems Talon cusps of secondary dentition, crowded and malpositioned teeth, gingivitis, natal teeth, hypo and hyper-dontia[] […] 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
  • Familial Hypophosphatemia

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

    Missing: Low Set Ears
  • 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[] Clinical features: flattened face with maxillary hypoplasia relative mandibular prognathism low set ears hypertelorism depressed nasal bridge high arched palate Short broad[] […] tooth-and-nail syndrome;tns;hypodontia-nail dysgenesis syndrome; tooth and nail syndrome; witkop syndrome Related symptoms: Autosomal dominant inheritance Abnormality of the dentition[]

  • 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).[] ears, and brachydactyly.[] Craniofacial and skeletal abnormalities are common, including brachycephaly, broad nasal bridge, flat midface, tented upper lip, synophrys, hypertelorism, abnormally shaped or low-set[]

    Missing: Delayed Dentition
  • Homocystinuria

    The patient shows some of the facial features that were already reported in the literature (high forehead, large floppy, low-set ears, flat philtrum and hypotonia of perioral[] , ectopia lentis, eczema, delayed dentition, fine hair, hemiplegia, infantile hypotonia, hypertonia, seizures, choreoathetosis, ataxia, dystonia, death Treatment: No effective[] (606887) Sulfite oxidase SUOX (12q13)* Biochemical profile: Elevated urine sulfite, thiosulfate, and S-sulfocysteine; decreased sulfate Clinical features: Developmental delay[]

    Missing: Absent Pulp Chambers
  • Autosomal-Recessive Non-Lethal Multiple Pterygium Syndrome

    Abnormalities of the head usually consist of epicanthal microcephaly, skin folds, long philtrum, antimongoloid palpebral slant, low-set ears, pointed and receding chin, ptosis[] PPS is associated with feeding difficulties, delayed language development, problems with dentition, maxillofacial development and learning difficulties.[] ears Low set ears Lowset ears [ more ] 0000369 Malignant hyperthermia 0002047 Micrognathia Little lower jaw Small jaw Small lower jaw [ more ] 0000347 Multiple pterygia 0001040[]

    Missing: Absent Pulp Chambers
  • Sanjad-Sakati Syndrome

    The facial features included microcephaly, thin lips, beaked nose, low set ears, and a retrognathic mandible.[] dentition and early decay, as well as small hands and feet.[] set ears / posteriorly rotated ears - Microcephaly - Micrognathia / retrognathia / micrognathism / retrognathism - Seizures / epilepsy / absences / spasms / status epilepticus[]

    Missing: Absent Pulp Chambers

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