Anesthetic care of Roberts syndrome: A Case report

10.5580/1651 ◽  
2010 ◽  
Vol 24 (2) ◽  
Keyword(s):  
Case Report ◽  
Anesthetic Care ◽  
Roberts Syndrome

scholarly journals Pneumothorax in a post-anesthetic care unit after right thyroidectomy with left neck dissection -A case report-

2010 ◽  
Vol 59 (6) ◽  
pp. 429 ◽  
Author(s):  
Sang Jun Lee ◽  
Dong-Jun Lee ◽  
Mun-Cheol Kim ◽  
Ui-Jae Im
Keyword(s):  
Case Report ◽  
Neck Dissection ◽  
Anesthetic Care ◽  
Left Neck

Care of the Neurosurgical Patient in the Post Anesthetic Care Unit

2001 ◽  
Vol 2 (3-4) ◽  
pp. 14-21
Author(s):  
Melissa McNeillis
Keyword(s):  
Intensive Care Unit ◽  
Intensive Care ◽  
Case Report ◽  
High Dependency Unit ◽  
Anesthetic Care ◽  
Anaesthetic Care ◽  
High Dependency ◽  
Neurosurgical Patient ◽  
Initial Care ◽  
Care Study

In this care study I will explain the care that SVB received following his admission to the Post Anaesthetic Care unit (PACU) and summarise his discharge to the Intensive Care Unit (ICU). The limitations that this case report presents are that often the care received in the PACU can be quite short in terms of total length of stay in hospital. It is not uncommon that High Dependency patients are received for initial care into the PACU following surgery and to be further discharged and nursed in either a dedicated High Dependency Unit or to the Intensive Care Unit.

The Roberts syndrome/SC phocomelia spectrum-A case report of an adult with review of the literature

2010 ◽  
Vol 152A (2) ◽  
pp. 472-478 ◽  
Author(s):  
Elaine Suk-Ying Goh ◽  
Chumei Li ◽  
Sheri Horsburgh ◽  
Yumi Kasai ◽  
Elena Kolomietz ◽  
...  
Keyword(s):  
Case Report ◽  
Review Of The Literature ◽  
Roberts Syndrome

scholarly journals Femoral-tibial-synostosis in a child with Roberts syndrome (Pseudothalidomide): a case report

Cases Journal ◽  
2008 ◽  
Vol 1 (1) ◽  
Author(s):  
Ali Al Kaissi ◽  
Robert Csepan ◽  
Klaus Klaushofer ◽  
Franz Grill
Keyword(s):  
Case Report ◽  
Roberts Syndrome

scholarly journals A Child with Roberts Syndrome: A Case Report

2017 ◽  
Vol 14 (2) ◽  
pp. 39-42
Author(s):  
Rajan K Sharma ◽  
Gopal R Sharma ◽  
Prakash Bista ◽  
Rajiv Jha
Keyword(s):  
Case Report ◽  
Recurrence Risk ◽  
Female Child ◽  
Craniofacial Anomalies ◽  
Craniofacial Abnormalities ◽  
Radiological Features ◽  
Limb Reduction ◽  
Roberts Syndrome ◽  
Genetically Determined ◽  
Number Of Individuals

Roberts syndrome is a genetically determined rare birth defect causing, skeletal deformities, particularly symmetrical limb reduction and craniofacial anomalies. For any child with limb and craniofacial bony malformations, this syndrome should be considered in the differentials. Although this syndrome represents only a small proportion of the total number of individuals with limb defi ciency, it is important to be identified in order to give accurate genetic counseling including recurrence risk in siblings and possible prenatal diagnosis. This is the case report of a 9 year old female child who presented with defective development of all four extremities and craniofacial abnormalities. The overall clinical and radiological features were suggestive of Roberts syndrome. Nepal Journal of Neuroscience, Vol. 14, No. 2,  2017 Page: 39-42

scholarly journals Anesthetic care for electroconvulsive therapy during pregnancy -A case report-

2011 ◽  
Vol 60 (3) ◽  
pp. 217 ◽  
Author(s):  
Hong-Seuk Yang ◽  
Hye-Jeong Seo ◽  
Yoon Kyung Lee
Keyword(s):  
Case Report ◽  
Electroconvulsive Therapy ◽  
Anesthetic Care
Sign in / Sign up

Export Citation Format

Share Document