Holt-Oram syndrome: Anesthetic challenges and safe outcome

Ann Card Anaesth. 2017 Jan-Mar;20(1):110-111. doi: 10.4103/0971-9784.197849.

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.

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / surgery
  • Adult
  • Androstanols
  • Anesthesia, Intravenous / methods*
  • Anesthetics, Intravenous
  • Carcinoma, Squamous Cell / complications
  • Carcinoma, Squamous Cell / surgery*
  • Fentanyl
  • Heart Defects, Congenital / complications*
  • Heart Defects, Congenital / surgery
  • Heart Septal Defects, Atrial / complications*
  • Heart Septal Defects, Atrial / surgery
  • Humans
  • Lower Extremity Deformities, Congenital / complications*
  • Lower Extremity Deformities, Congenital / surgery
  • Male
  • Neuromuscular Blockade / methods*
  • Neuromuscular Nondepolarizing Agents
  • Propofol
  • Rocuronium
  • Tongue / surgery
  • Tongue Neoplasms / complications
  • Tongue Neoplasms / surgery*
  • Upper Extremity Deformities, Congenital / complications*
  • Upper Extremity Deformities, Congenital / surgery

Substances

  • Androstanols
  • Anesthetics, Intravenous
  • Neuromuscular Nondepolarizing Agents
  • Fentanyl
  • Rocuronium
  • Propofol

Supplementary concepts

  • Holt-Oram syndrome