Literature DB >> 7609307

[Anesthetic management of Seckel syndrome: a case report].

N Shiraishi1, K Takakuwa, N Yamamoto, R Kitamoto, Y Sakaguchi.   

Abstract

Seckel syndrome is a rare syndrome of chromosome aberration, in which bird-headed dwarfism, microcephalus and other minor deformities are recognized. A 24-year-old male patient with Seckel syndrome underwent both abdominal and orthopaedic surgeries in 1 year under general anesthesia. The first operation was an emergent operation under preshock state and enterostomy was performed. The second was arthrodesis of the hip joint. Before the second operation, laryngeal CT, tomography and fiberscopy revealed stenosis just below his vocal cord. During the second operation, the anesthesia was unsatisfactory with inhalation of nitrous oxide and sevoflurane and intravenous vecuronium, because of intraoperative abnormal hypertension. But the recovery from the anesthesia was prompt. Although we experienced no difficulty in intubation except for intraoperative abnormal hypertension, preoperative laryngeal and renal examinations are necessary in the anesthetic management of this syndrome.

Entities:  

Mesh:

Year:  1995        PMID: 7609307

Source DB:  PubMed          Journal:  Masui        ISSN: 0021-4892


  1 in total

1.  Anesthetic management of a child with Seckel syndrome for multiple extractions and restoration of teeth.

Authors:  Suman Arora; Babita Ghai; Vidya Rattan
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2012-07
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.