Aperts syndrom or "craniosynostosis syndromes" Treff i utvalgte kilder: [Skjul boksen]
  1. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/434/differentials
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    ... syndrome Craniofacial abnormalities (e.g., Pierre Robin, Crouzon, Apert syndromes) History Exam 1st investigation Other investigations babies with ... ear-canal abnormalities may be present on otoscopy; Apert: syndactyly of hands and feet, characteristic facies with wide-set eyes and low-set ears, ear-canal abnormalities may be present on otoscopy ... investigation Other investigations ...
  2. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/434/differentials
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    ... abnormalities (e.g., Pierre Robin's, Crouzon's, Apert's syndromes) History Exam 1st investigation Other investigations babies with ... abnormalities (e.g., Pierre Robin's, Crouzon's, Apert's syndromes) History Exam 1st investigation Other investigations babies with ...
  3. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/434/pdf/434.pdf
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    ... a syndrome, such as Crouzon, Pierre Robin, or Apert syndromes. Crouzon is a genetic syndrome inherited in an ... defect in development and is characterized by micrognathia. Apert syndrome is a branchial arch disorder resulting in developmental ...
  4. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/434/aetiology
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    ... a syndrome, such as Crouzon, Pierre Robin, or Apert syndromes. Crouzon is a genetic syndrome inherited in an ... defect in development and is characterized by micrognathia. Apert syndrome is a branchial arch disorder resulting in developmental ...
  5. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/434/pdf/434.pdf
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    ... such as Crouzon's, Pierre Robin's, or Apert's syndromes. Crouzon's is a genetic syndrome inherited in ... defect in development and is characterised by micrognathia. Apert's syndrome is a branchial arch disorder resulting in developmental ...
  6. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/781/history-exam
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    ... such as Robin sequence and Collins, Pfeiffer, and Apert syndromes. [38] Sher AE. Mechanisms of airway obstruction in ... Perloff WH et al. Obstructive sleep apnea in Apert's and Pfeiffer's syndromes: more than a craniofacial abnormality. Plast Reconstr Surg. ...
  7. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/781/pdf/781.pdf
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    ... such as Robin sequence and Collins, Pfeiffer, and Apert syndromes. [ 38] [ 39] [ 50] [ 51] [ 52] adenotonsillar hypertrophy (obstructive ... Perloff WH et al. Obstructive sleep apnea in Apert's and Pfeiffer's syndromes: more than a craniofacial abnormality. Plast Reconstr Surg. ...
  8. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/781/history-exam
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    ... as Robin's sequence and Collins, Pfeiffer, and Apert syndromes. [38] Sher AE. Mechanisms of airway obstruction in ... Perloff WH et al. Obstructive sleep apnea in Apert's and Pfeiffer's syndromes: more than a craniofacial abnormality. Plast Reconstr Surg. ...
  9. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/781/pdf/781.pdf
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    ... as Robin's sequence and Collins, Pfeiffer, and Apert syndromes. [ 38] [ 39] [ 50] [ 51] [ 52] adenotonsillar hypertrophy (obstructive ... Perloff WH et al. Obstructive sleep apnea in Apert's and Pfeiffer's syndromes: more than a craniofacial abnormality. Plast Reconstr Surg. ...
  10. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/689/aetiology
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    ... finding in craniofacial syndromes (e.g., Crouzon and Apert syndromes) and craniosynostosis, due to the abnormal orientation of ...
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