Management of neuroendocrine tumor in a patient with Rubinstein-Taybi syndrome in chronic hemodialysis
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چکیده
منابع مشابه
patellofemoral ligament reconstruction in a patient with rubinstein-taybi syndrome.
recurrent dislocation of patella may occur in patients with ligament laxity. method of treatment in this condition is controversial but patellofemoral ligament reconstruction is the most accepted method. we present a patient with rubinstein-taybi syndrome and recurrent patellar dislocation who managed successfully by patellofemoral ligament reconstruction.
متن کاملPatellofemoral ligament reconstruction in a patient with Rubinstein-Taybi syndrome.
Recurrent dislocation of patella may occur in patients with ligament laxity. Method of treatment in this condition is controversial but patellofemoral ligament reconstruction is the most accepted method. We present a patient with Rubinstein-Taybi syndrome and recurrent patellar dislocation who managed successfully by patellofemoral ligament reconstruction.
متن کاملManagement of Anesthesia for Rubinstein-Taybi syndrome
Corresponding author: Cheon-Hee Park, M.D., Department of Anesthesia and Pain Medicine, Gwangju Christian Hospital, 37, Yangnim-ro, Nam-gu, Gwangju 503-715, Korea. Tel: 82-62-650-5154, Fax: 82-62-650-5116, E-mail: [email protected] This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http:// creativecommons.org/licenses/by-nc/3...
متن کاملRubinstein-Taybi syndrome with scoliosis
STUDY DESIGN Case report. OBJECTIVE The authors present the case of a 14-year-old boy with Rubinstein-Taybi syndrome (RSTS) presenting scoliosis. SUMMARY OF BACKGROUND DATA There have been no reports on surgery for RSTS presenting scoliosis. METHODS The patient was referred to our hospital for evaluation of a progressive spinal curvature. A standing anteroposterior spine radiograph at pre...
متن کاملRubinstein-Taybi Syndrome with Psychosis
Rubinstein-Taybi syndrome is characterized by a broad thumb and bulbous hallux, short stature, intellectual disability and distinctive facial features [1]. It is a rare neuro-developmental disorder with a reported prevalence of 1 in 1,25,000 births [2]. Psychosis in RTS is highly infrequent with only a few scattered case reports [3]. A comprehensive literature search yielded only one case repor...
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ژورنال
عنوان ژورنال: Nefrología (English Edition)
سال: 2018
ISSN: 2013-2514
DOI: 10.1016/j.nefroe.2018.05.001