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Growth reference charts for children with hypochondroplasia. pubmed.ncbi.nlm.nih.gov/37814549/ Thank you to all the families with hypochondroplasia that contributed growth data to make this possible!!

#Glucocorticoids, #zebrafish and #Brain - what juicy combination! journals.biologists.com/dmm/article/16…

Calling all paediatricians - we have been largely watching from afar re the role of PAs in other specialties. RCPCH now wants to know what we think - really important we fill this in: forms.office.com/pages/response…

Would you help us by taking part in this important survey? We are looking for people to give us their thoughts on #raredisease education! 🦓 Your thoughts really matter and we want to hear from you. Tap on the link to get started! forms.gle/ezWfd1oH3zSJN5…

Delighted with this research award for our study “Collaborative devt of national education standards & resources for emerg. mgt of adrenal insufficiency: mixed-model multiphase study” led by Lucy Bray #BSPED2023 Prof May Ng OBE 吳 诗 梅 Addison's Disease Self-Help Group (ADSHG) The Pituitary Foundation BSPED

👏Congratulations to Li Chan Queen Mary University of London, one of our Senior Editors on winning the Society for Endo Starling Medal for contributing to exceptional scientific advances in #endocrinology. At #SfeBES2023 Dr Chan explores Melanocortin Receptors & their accessory proteins in health & disease.

What a fantastic meeting! Making friends across the pond. 🇺🇸🇬🇧 Autumn UK Skeletal Dysplasia Meeting: “Stick or Twist” Larsen Syndrome, Multiple Synostoses Syndromes and so much more!

The BBS & friends in the Rare Bone Alliance celebrated the launch of the NHS Rare Disease Collaborative Network for Adult Rare Bone. It was a successful day of networking and informative talks with reps from the 19 NHS Hospitals who have joined! Read more: shorturl.at/jzI28

@UkXlh Daily Mail Health Ethan Ennals Rebecca Whittaker Pleading for help here! Genetic Alliance UK Rare Disease UK

SDMC Denver

SDMC working hard 2023

There are still a few places left on the ISCBH/European Reference Network on Rare Bone Diseases Achondroplasia workshop at #ICCBH2024 so register soon! theiscbh.org/iccbh/iccbh-20…

Just 4 days to go until #ICCBH2024 and it's not too late to register!

Natural history of spinal cord compression stage AFMS3 in infants with achondroplasia 40% progress and undergo neurosurgery Suggest all have MRI at 6m Retrospective cohort study 🇬🇧 Prof Amaka C Offiah Great Ormond Street Neurosurgery adc.bmj.com/content/early/…

ADC Great Ormond Street Neurosurgery Great work led by Moira Cheung concluding that all infants with achondroplasia AFMS3 should have MRI at 6m of age.