P 1111. Case Report of a Juvenile Patient with Niemann–Pick’s Disease Type C

2018 ◽  
Author(s):  
Nathalie Frank ◽  
Jochen Baumkötter
2001 ◽  
Vol 39 (11) ◽  
pp. 971-974 ◽  
Author(s):  
A R. J Schneider, MD ◽  
F Stichling, MD ◽  
M Hoffmann, MD ◽  
R Scheler, MD ◽  
J C Arnold, MD ◽  
...  

2019 ◽  
Vol 43 (5) ◽  
pp. 621-624
Author(s):  
Eun Jae Ko ◽  
In Young Sung ◽  
Han-Wook Yoo

2021 ◽  
Vol 55 (4) ◽  
pp. 238-241
Author(s):  
Rejane Viana dos Santos ◽  
Tamila das Neves Ferreira ◽  
Daniela Oliveira de Almeida ◽  
Lilian Brito da Silva Fatal ◽  
Edilene Maria Queiroz Araujo

Abstract Objectives. We aim to report the clinical repercussions of a nutritional approach in a patient diagnosed with Niemann Pick disease type C (NPC) using miglustat as pharmacological therapy. Case report. A 33-year-old woman diagnosed with NPC using miglustat was instructed to look for a dietary management at our nutrition service. Patient’s symptoms were weight loss and important gastrointestinal alterations. Our nutritional prescription was a high-calorie and high-protein, lactose- and sucrose-free diet, as well as a daily supplementation of L-glutamine, probiotics, omega 3, and coenzyme Q10. After two months, the patient had weight gain and improvement in the intestinal health. Conclusions. We found that nutritional prescription aided in the treatment of NPC and revealed that nutritional care represents an important strategy in the management of rare genetic diseases.


1993 ◽  
Vol 38 (5) ◽  
pp. 368-369
Author(s):  
Emmanuel Stip ◽  
Jocelyne Coumoyer ◽  
Pierre Léouffre ◽  
Gérard Cournoyer

1973 ◽  
Vol 4 (02) ◽  
pp. 207-225 ◽  
Author(s):  
A. Anzil ◽  
K. Blinzinger ◽  
P. Mehraein ◽  
S. Dozic

1994 ◽  
Vol 11 (1) ◽  
pp. 34-38 ◽  
Author(s):  
Fiona Gaughran ◽  
Catherine Keohane ◽  
Mary Buckley

AbstractThe clinical and pathological features are described in a case of prolonged dementia in a 59 year old man with familial dementia and extrapyramidal disorder. Postmortem examination showed severe fronto-temporal and basal ganglia atrophy, with many “ballooned neurons” in the residual cortex most likely representing Pick's disease. The differential diagnosis is discussed and aspects of this rare condition are reviewed.


2018 ◽  
Vol 39 (6) ◽  
pp. 1015-1019 ◽  
Author(s):  
Stefano Tozza ◽  
Raffaele Dubbioso ◽  
Rosa Iodice ◽  
Antonietta Topa ◽  
Marcello Esposito ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document