Growth Hormone Therapy in Adults With Prader-Willi Syndrome Growth Hormone Therapy in Adults With Prader-Willi Syndrome
Should growth hormone therapy have a role in the management of adults with Prader-Willi syndrome?Clinical Endocrinology (Source: Medscape Today Headlines)
Source: Medscape Today Headlines - April 29, 2021 Category: Consumer Health News Tags: Diabetes & Endocrinology Journal Article Source Type: news
Dietary Macronutrient Regulations in Prader-Willi Syndrome Dietary Macronutrient Regulations in Prader-Willi Syndrome
How are appetite-regulating hormones among children with Prader-Willi syndrome impacted by dietary macronutrients?Clinical Endocrinology (Source: Medscape Today Headlines)
Source: Medscape Today Headlines - December 11, 2020 Category: Consumer Health News Tags: Diabetes & Endocrinology Journal Article Source Type: news
Assessing cost of Prader-Willi syndrome in the US
(Source: PharmacoEconomics and Outcomes News)
Source: PharmacoEconomics and Outcomes News - May 31, 2020 Category: Drugs & Pharmacology Source Type: news
New drug shows potential to reduce ghrelin levels
A new drug undergoing worldwide trials shows potential to reduce ghrelin levels in patients with Prader-Willi syndrome.Scienmag (Source: Society for Endocrinology)
Source: Society for Endocrinology - January 6, 2020 Category: Endocrinology Source Type: news
Drug trial seeking first ever treatment for dangerous side effect of Prader-Willi syndrome
(Michigan Medicine - University of Michigan) A worldwide research effort is underway for finding a treatment option for hyperphagia, the most common genetic cause of life-threatening childhood obesity. (Source: EurekAlert! - Medicine and Health)
Source: EurekAlert! - Medicine and Health - January 3, 2020 Category: International Medicine & Public Health Source Type: news
The children at risk of eating themselves to death
"One sweet here, another one there - that could kill him," says a man whose son has Prader-Willi syndrome. (Source: BBC News | Health | UK Edition)
Source: BBC News | Health | UK Edition - December 26, 2019 Category: Consumer Health News Source Type: news
Levo Therapeutics Receives Fast Track Designation From FDA for Intranasal Carbetocin for the Treatment of Prader-Willi Syndrome
Announces Completion of Series B Financing
CHICAGO, Nov. 18, 2019 -- (Healthcare Sales & Marketing Network) -- Levo Therapeutics, Inc. announced today that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for LV-101 (intra... Biopharmaceuticals, Neurology, Drug Delivery, FDA Levo Therapeutics, Intranasal, Carbetocin, Prader-Willi Syndrome (Source: HSMN NewsFeed)
Source: HSMN NewsFeed - November 18, 2019 Category: Pharmaceuticals Source Type: news
Toddler has surgery to straighten his spine after its 90° curve crushed his lung
Osian Llewellyn, from South Wales, was diagnosed with Prader-Willi syndrome when he was two-and-a-half. This caused him to have weak muscles, which provide his spine with 'no support' (Source: the Mail online | Health)
Source: the Mail online | Health - September 19, 2019 Category: Consumer Health News Source Type: news
Mother is constantly accused of overfeeding four-year-old son who weighs 112 POUNDS
Trinity Leonard, from Washington state is convinced her son Peter has Prader-Willi syndrome, which is thought to affect one in every 15,000 people. (Source: the Mail online | Health)
Source: the Mail online | Health - September 5, 2019 Category: Consumer Health News Source Type: news
What Does the General Pediatrician Do When There Are Concerns for a Rare Disease?
Discussion
Bardet-Biedl syndrome (BBS) is a rare disorder. It is usually considered an autosomal recessive disorder but there is significant intra-familial variability. There are multiple genes (~20 currently) involved and it is believed that the phenotypic variability is due to “…differences in the total mutational load across different BBS associated genes….” It is a ciliopathy where mutation changes in proteins in the cilias causes problems in the cilia’s functioning particularly signaling. Cilia are important in signaling to maintain tissue and cellular homeostasis. Obviously screening of ...
Source: PediatricEducation.org - August 19, 2019 Category: Pediatrics Authors: pediatriceducationmin Tags: Uncategorized Source Type: news
Prader-Willi Syndrome: Overview Video Prader-Willi Syndrome: Overview Video
Osmosis (Source: Medscape Today Headlines)
Source: Medscape Today Headlines - July 19, 2019 Category: Consumer Health News Tags: Med Students Commentary Source Type: news
A Pioneering Treatment for Uncontrollable Hunger
A special diet and growth hormones may offer hope for children with Prader-Willi syndrome. (Source: NYT Health)
Source: NYT Health - June 3, 2019 Category: Consumer Health News Authors: Jane E. Brody Tags: Prader-Willi Syndrome Genetics and Heredity Children and Childhood Parenting Weight Source Type: news
Growth hormone safe to treat sufferers of Prader-Willi Syndrome
According to a study published inThe Journal of Clinical Endocrinology and Metabolism, growth hormone treatment has no negative effect on patients with Prader-Willi Syndrome and associated sleep-related breathing disorders.Endocrinology Advisor (Source: Society for Endocrinology)
Source: Society for Endocrinology - May 9, 2019 Category: Endocrinology Source Type: news
Effects of Carbohydrate Restriction in Prader-Willi Syndrome Effects of Carbohydrate Restriction in Prader-Willi Syndrome
A new study compares the concentrations of hormones and metabolites among Prader-Willi children who consumed either a low carbohydrate or a low-fat diet. How did they differ?Clinical Endocrinology (Source: Medscape Today Headlines)
Source: Medscape Today Headlines - April 22, 2019 Category: Consumer Health News Tags: Diabetes & Endocrinology Journal Article Source Type: news
UConn and Foundation for Prader Willi Research create stem cell biobank
(University of Connecticut) A new collaboration between UConn Health and the Foundation for Prader-Willi Research will create a centralized, high quality biobank of stem cells to help researchers better understand Prader-Willi syndrome, a rare genetic disease that may hold insights into obesity, developmental delays, autism spectrum disorders, and many other conditions. (Source: EurekAlert! - Medicine and Health)
Source: EurekAlert! - Medicine and Health - April 9, 2019 Category: International Medicine & Public Health Source Type: news
