CONTENT HUB

Stay up to date with the release of new educational materials on melanocortin-4 receptor (MC4R) pathway diseases.

Content Library

Use the buttons below to filter materials based on your interests.

Mini Slide Deck: Clinical and molecular diagnosis of Bardet-Biedl syndrome

Solarat C, Valverde D.

Mini-slide deck

Sign in to download PDF

Mini-slide deck: Genetic contributors to obesity

Sivasubramanian R, Malhotra S

Mini-slide deck

Sign in to download PDF

Explainer animation: Caregiver burden in Bardet‑Biedl syndrome: findings from the CARE‑BBS study

Dr Elizabeth Forsythe

Video

Login to watch

Explainer Animation: Burden of hyperphagia and obesity in Bardet-Biedl syndrome: a multicountry survey

Dr Elizabeth Forsythe

Video

Login to watch

Explainer animation: Clinical and molecular diagnosis of Bardet-Biedl syndrome

Solarat C, Valverde D.

Video

Login to watch

Got a specific question?

If you can't find what you're looking for, or want to discuss a topic in more detail, reach out to our team.

Discover important information relating to the field of MC4R pathway diseases in the latest edition of The MC4R Journal below

This edition of The MC4R Journal highlights four scientific articles relevant to the field of rare MC4R pathway diseases. Each article is accompanied with an explanatory mini-slide deck, infographic and animation, each of which can be accessed via the links below.  

Sign up to receive future editions of this newsletter directly.

MC4R Journal

Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study

The CARE-BBS study reports on the caregiver burden associated with hyperphagia and obesity among patients with BBS. A multi-country survey was used to quantify the caregiver burden, which was found to be multifaceted and complex.

Forsythe E, et al. Orphanet J Rare Dis. 2023;18(1):181.

MC4R Journal

Burden of hyperphagia and obesity in Bardet-Biedl syndrome: a multicountry survey

Research into the impact of hyperphagia on the lives of caregivers and patients with BBS has been limited, until now. The CARE-BBS study launched a multi-country survey to quantify the physical and emotional burden associated with hyperphagia in BBS, which was described amongst others as "broad" and "negative".

Forsythe E, et al. Orphanet J Rare Dis. 2023;18(1):182.

MC4R Journal

Clinical and molecular diagnosis of Bardet-Biedl syndrome

This article explores the extensive clinical heterogeneity and main features of BBS. It aims to define the role of the different BBS genes and discuss various strategies for the clinical and molecular diagnosis of BBS.

Solarat C, Valverde D. Methods in Cell Biology. 2023;176:125–137.

MC4R Journal

Genetic contributors to obesity

The current research landscape of obesity caused by genetic impairments is summarised in this article. There is a focus on the known prevalence and hidden burden of obesity caused by genetic impairments, genetic drivers of appetite regulation, the importance of genetic testing and clinical features of monogenic and syndromic obesity.

Sivasubramanian R, Malhotra S. Gastroenterol Clin N Am. 2023;52:323–332.

MC4R Journal

Caregiver burden in Bardet-Biedl syndrome: findings from the CARE-BBS study

The CARE-BBS study reports on the caregiver burden associated with hyperphagia and obesity among patients with BBS. A multi-country survey was used to quantify the caregiver burden, which was found to be multifaceted and complex.

Forsythe E, et al. Orphanet J Rare Dis. 2023;18(1):181.

01

04

Check out our events for 2024

On-demand webinar

Understanding hyperphagia: a root cause, recognition & burden

During this Rhythm-sponsored webinar, Professor Carel Le Roux and Professor Martin Wabitsch explore the role of the MC4R pathway in hyperphagia and early-onset, severe obesity, including a patient perspective on the real-life burden of living with hyperphagia.

Watch now

01

03

Join our community of healthcare professionals

  • Get the latest news
  • Access materials within the Content Hub
  • Hear about upcoming events
  • Receive recommended content based on your interests