scholarly journals Adult Noonan’s syndrome and associated severe scoliosis. A case report and discussion of the anaesthetic implications.

Author(s):  
Keevan Singh ◽  
Candice Ramdin

Noonan’s syndrome is a relatively rare genetic disorder with distinct clinical manifestations. Surgery is usually required early on in life however many of these patients can present for surgery later in life. Specific challenges to the anaesthesia can include, coexistent cardiac abnormalities, risk of difficult intubation, bleeding abnormalities, scoliosis and the potential for triggering Malignant Hyperthermia. Although characteristic phenotypical appearances can become less distinct with age, many abnormalities persist along with new potential problems. We report a case of an adult male with Noonan’s syndrome who developed severe scoliosis and presented for elective hemorrhoid repair. The procedure was safely performed under low dose spinal saddle anaesthesia. We also review the relevant perioperative issues and the challenges that can be encountered when deciding on the most appropriate mode of anaesthesia.

1991 ◽  
Vol 40 (1) ◽  
pp. 443-447
Author(s):  
Masaki Takahashi ◽  
Nobuyuki Ito ◽  
Masao Eto ◽  
Yuuzo Ohta ◽  
Katsuro Iwasaki

2007 ◽  
Vol 30 (4) ◽  
pp. 644-644
Author(s):  
K. M. Maksym ◽  
E. Romejko-Wolniewicz

2017 ◽  
Vol 41 (S1) ◽  
pp. S434-S434
Author(s):  
R. Cosme ◽  
S. Dharmapuri

This case report describes the successful use of low dose quetiapine in the treatment of agitation in a patient with Treacher–Collins syndrome (TCS) and suspected autistic spectrum disorder (ASD). Results from this case report found better efficacy in controlling symptoms of agitation in ASD utilizing lower doses of quetiapine. TCS is a genetic disorder that is characterized by a mandibulofacial dysostosis but is not associated with developmental delay, nor is it associated with a high risk of co-morbid autism, and to our knowledge, there are no previous reports of a co-occurrence of TCS and ASD in the extant literature. There are reports of mandibulofacial dysostosis associated with co-morbid developmental delay that are similar but distinct from TCS, however these reports do not comment on the treatment of agitation in this patient population. The results described in this case report demonstrate a reduction of agitation with low dose quetiapine, and offers support for the reconceptualization of agitation in ASD as a primary affective dysregulation which is also in line with evidence from the extant literature regarding the neurobiologic basis of aggression.Disclosure of interestThe authors have not supplied their declaration of competing interest.


Microsurgery ◽  
2009 ◽  
Vol 29 (6) ◽  
pp. 486-489 ◽  
Author(s):  
Nektarios Sinis ◽  
Tatjana Ismini Lanaras ◽  
Armin Kraus ◽  
Frank Werdin ◽  
Hans-Eberhard Schaller ◽  
...  

Neurocirugía ◽  
2007 ◽  
Vol 18 (3) ◽  
pp. 241-246 ◽  
Author(s):  
P.D. Delgado-López ◽  
V. Martín-Velasco ◽  
A.Mª. Galacho-Harriero ◽  
J.M. Castilla-Díez ◽  
A. Rodríguez-Salazar ◽  
...  

2003 ◽  
Vol 18 (1) ◽  
pp. 68-72 ◽  
Author(s):  
Pinar Isik Agras ◽  
Esra Baskin ◽  
A. Ebru Sakallioglu ◽  
I. Serdar Arda ◽  
Sükriye Ayter ◽  
...  

Neurocirugía ◽  
2007 ◽  
Vol 18 (3) ◽  
Author(s):  
P.D. Delgado-López ◽  
V. Martín-Velasco ◽  
A.Mª. Galacho-Harriero ◽  
J.M. Castilla-Díez ◽  
A. Rodríguez-Salazar ◽  
...  

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