Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Monica Drivdal"'
Publikováno v:
Health and Quality of Life Outcomes, Vol 16, Iss 1, Pp 1-10 (2018)
Abstract Background LCS1 (Lymphedema Cholestasis Syndrome 1/Aagenaes syndrome) is a rare, hereditary disorder, where the highest known prevalence is in Norway. The disorder is characterized by lymphedema and periodic cholestasis from birth or the neo
Externí odkaz:
https://doaj.org/article/e73952fdac5d41068614ef208546d0e9
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 78:566-574
The risks of developing energy or nutrient deficits are of great concern in infants and children with the rare lymphoedema cholestasis syndrome 1 (LCS1)/Aagenaes syndrome. In adolescents and adults, it is not known whether LCS1 patients need specific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3b40b972d60649a50758f4cda82b53e
https://doi.org/10.1080/00365513.2018.1519723
https://doi.org/10.1080/00365513.2018.1519723
Publikováno v:
Special Care in Dentistry. 35:83-89
Aagenaes syndrome/lymphedema cholestasis syndrome 1 (LCS1) is a rare genetic disorder characterized by neonatal cholestasis and lymphedema. The aim was to assess dental care and oral health in adults with LCS1. Fifteen (9M, 6F) individuals diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce553d17fc36315bb921beb8419ce15c
https://doi.org/10.1111/scd.12080
https://doi.org/10.1111/scd.12080
Publikováno v:
Scandinavian Journal of Gastroenterology. 41:465-471
Objective. To investigate the prognosis of liver disease in Aagenaes syndrome (lymphoedema cholestasis syndrome 1 (LCS1)), which is an autosomal recessive inherited syndrome consisting of neonatal cholestasis with intermittent cholestatic episodes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cf6496840a781c3380e5fceacfdd715
https://doi.org/10.1080/00365520500335183
https://doi.org/10.1080/00365520500335183
Publikováno v:
Lymphatic research and biology. 12(4)
The characterizations of primary lymphedemas in different hereditary diseases are often published as case reports. In this study, 17 out of 20 Norweigian adult patients with lymphedema cholestasis syndrome 1 (LCS1)/Aagenaes syndrome were examined. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f265f1296fc69753e7126ddcab232d07
https://pubmed.ncbi.nlm.nih.gov/25317502
https://pubmed.ncbi.nlm.nih.gov/25317502
Publikováno v:
Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry. 35(2)
Aagenaes syndrome/lymphedema cholestasis syndrome 1 (LCS1) is a rare genetic disorder characterized by neonatal cholestasis and lymphedema. The aim was to assess dental care and oral health in adults with LCS1. Fifteen (9M, 6F) individuals diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5873936b111ce21239f36928e297533
https://pubmed.ncbi.nlm.nih.gov/25039919
https://pubmed.ncbi.nlm.nih.gov/25039919
Publikováno v:
Clinical nutrition (Edinburgh, Scotland). 29(4)
summary Background&Aims: Patients with lymphoedema cholestasis syndrome 1/Aagenaes Syndrome need a fat reduced diet when cholestatic. We wanted to assess the need for dietary counselling outside cholestatic episodes, and hypothetized that no counsell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07c986c598fed1f98049978c9a7cc23d
https://pubmed.ncbi.nlm.nih.gov/20170991
https://pubmed.ncbi.nlm.nih.gov/20170991