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 ... syndrome Craniofacial abnormalities (e.g., Pierre Robin, Crouzon, Apert syndromes) History Exam 1st investigation Other investigations babies with ...
  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 syndrome. Crouzon is a genetic syndrome inherited in an ... reserved. OVERVIEW Evaluation of hearing loss Overview micrognathia. Apert syndrome is a branchial arch disorder resulting in developmental ...
  4. nokc-helsebiblioteket-collection
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    https://www.helsebiblioteket.no/.../obstruktiv-sovn-apne
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    ... deformiteter/avvik, som Treacher Collins syndrom, Crouzon syndrom, Apert syndrom, Pierre Robins sekvens, Beckwith Wiedemanns syndrom, Akondroplasi, Chiari ...
  5. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-us/434
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    ... syndrome Craniofacial abnormalities (e.g., Pierre Robin, Crouzon, Apert syndromes) Waardenburg syndrome Acoustic neuroma (vestibular schwannoma) Glomus tumor ...
  6. 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 syndrome. 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 ...
  7. RELIS
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    relis.arnett.no/Utredning_Ekstern.aspx?Relis=3&S=7971
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    ... Downs syndrom, atopisk dermatitt, retinitis pigmentosa, Marfans syndrom, Aperts syndrom og Ehlers-Danlos syndrom (1). I WHOs bivirkningsdatabase ...
  8. nokc-helsebiblioteket-collection
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    https://www.helsebiblioteket.no/.../avvikende-hodeform
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    ... også misdannelser i andre organsystemer. Muenke, Crouzon og Apert syndrom er eksempler på syndromale kraniosynostoser. Vedr. kraniofaciale misdannelser ...
  9. bmj-bestpractice
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    https://bestpractice.bmj.com/topics/en-gb/434/pdf/434.pdf
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    ... Assessment of hearing loss Overview Robin's, or Apert's syndrome. 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 ...
  10. 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. ...
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