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Holt-Oram syndrome: Anesthetic challenges and safe outcome.

Abstract
Holt-Oram syndrome (HOS) is an autosomal dominant disease with skeletal and cardiac manifestations. We here are presenting a 31-year-old man and a diagnosed case of HOS, with an ulceroproliferative lesion on lateral border of the tongue, was posted for wide excision of lesion with primary closure and left side radical neck dissection.
AuthorsMeenal Rana, Sohan Lal Solanki, Vandana Agarwal, Jigeeshu V Divatia
JournalAnnals of cardiac anaesthesia (Ann Card Anaesth) 2017 Jan-Mar Vol. 20 Issue 1 Pg. 110-111 ISSN: 0974-5181 [Electronic] India
PMID28074809 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Androstanols
  • Anesthetics, Intravenous
  • Neuromuscular Nondepolarizing Agents
  • Fentanyl
  • Rocuronium
  • Propofol
Topics
  • Abnormalities, Multiple (surgery)
  • Adult
  • Androstanols
  • Anesthesia, Intravenous (methods)
  • Anesthetics, Intravenous
  • Carcinoma, Squamous Cell (complications, surgery)
  • Fentanyl
  • Heart Defects, Congenital (complications, surgery)
  • Heart Septal Defects, Atrial (complications, surgery)
  • Humans
  • Lower Extremity Deformities, Congenital (complications, surgery)
  • Male
  • Neuromuscular Blockade (methods)
  • Neuromuscular Nondepolarizing Agents
  • Propofol
  • Rocuronium
  • Tongue (surgery)
  • Tongue Neoplasms (complications, surgery)
  • Upper Extremity Deformities, Congenital (complications, surgery)

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