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4,045 Possible Causes for Absent Pulp Chambers, Failure to Thrive, 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).[] In infancy there are feeding problems, failure to thrive, hypotonia (floppiness), prolonged napping and lethargy.[] ears, and brachydactyly.[]

  • Donohue Syndrome

    The clinical course showed failure to thrive, and episodes of alternating hypoglycemia and hyperglycemia. Laboratory tests revealed direct hyperbilirubinemia.[] The patient showed typical "elfin-like" face with wide nostrils and thick lips, large and low-set ears, and dysplastic nails.[] DS is characterized by pre- and postnatal growth retardation with failure to thrive, lipoatrophy, muscle wasting, acanthosis nigricans, hypertrichosis, and dysmorphic features[]

    Missing: Absent Pulp Chambers
  • Homocystinuria

    […] to thrive, neurological abnormalities, and others depending on the cause.[] 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[] There was no significant past history of mental retardation, failure to thrive, or seizure disorder as reported in classic cases of cblC.[]

    Missing: Absent Pulp Chambers
  • Cerebro-Oculo-Facio-Skeletal Syndrome

    […] to thrive.[] She was having microcephaly, micrognathia, micro-ophthalmia, large low set ears, upper lip overhanging the lower lip and congenital contractures.[] Symptoms may include large, low-set ears, small eyes, microcephaly (abnormal smallness of the head), micrognathia (abnormal smallness of the jaws), clenched fists, wide-set[]

    Missing: Absent Pulp Chambers
  • Noonan Syndrome

    […] to thrive, short stature, feeding difficulties, sternal deformity, renal malformation, pubertal delay, cryptorchidism, developmental or behavioral problems, vision problems[] . - It is difficult to look high in the sky at noon, therefore everything is down in NOONan syndrome- Low set ears, Downslanting eyes, Low posterior hair line, Low levels[] The patient presented with postnatal-onset failure-to-thrive, developmental delay, microcephaly, velopalatal incompetence, pectus excavatum, coarctation of aorta, atrial and[]

    Missing: Absent Pulp Chambers
  • Sanjad-Sakati Syndrome

    We encountered a 2-year-old boy with hypocalcemia, failure to thrive and macrocytic anemia.[] The facial features included microcephaly, thin lips, beaked nose, low set ears, and a retrognathic mandible.[] set ears / posteriorly rotated ears - Microcephaly - Micrognathia / retrognathia / micrognathism / retrognathism - Seizures / epilepsy / absences / spasms / status epilepticus[]

    Missing: Absent Pulp Chambers
  • Costello Syndrome

    We present a 7 months old child with severe failure to thrive whose "subtle" facial dysmorphism at the time eluded clinical recognition of the syndrome.[] Costello syndrome is an autosomal dominant disorder comprising growth deficiency, mental retardation, curly hair, coarse facial features, nasal papillomata, low-set ears with[] His clinical findings were sparse, thin, and light-colored hair, bilateral ptosis, low-set ears, depressed nasal bridge, bulbous nose, short neck, loose pigmented skin with[]

    Missing: Absent Pulp Chambers
  • Turner Syndrome

    […] to thrive in infancy Faltering weight in infancy Weight faltering in infancy [ more ] 0001531 Genu valgum Knock knees 0002857 Hashimoto thyroiditis 0000872 Hearing impairment[] Other characteristics, like widely spaced nipples or low-set ears, also may lead to a suspicion of Turner syndrome.[] […] to thrive.[]

    Missing: Absent Pulp Chambers
  • Hallermann-Streiff Syndrome

    She had a history of severe snoring, reported nocturnal apnea, excessive daytime hypersomnolence, nocturnal enuresis, and failure to thrive.[] We describe a 20-year-old female patient whose clinical findings mostly fall into this syndrome, except for the presence of slightly low-set ears.[] A 2-mo-old female baby presented with ocular abnormalities and severe failure to thrive since birth. The clinical features were compatible with the diagnosis of HSS.[]

    Missing: Absent Pulp Chambers
  • Wolf-Hirschhorn Syndrome

    Accordingly, prenatal-onset growth retardation and failure to thrive have been found to result from haploinsufficiency for a 4p gene located between 0.4 and 1.3 Mb, whereas[] ears.[] Clinical manifestations of WHS include intrauterine growth restriction, failure to thrive in the neonatal period that is present simultaneously with hypotonia, typical "Greek[]

    Missing: Absent Pulp Chambers

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