Search results for #congenitaladrenalhyperplasia
@Stephen40017241 @Invisible_TSW @Stephen40017241 Females with Y-chromosomes: E.g. #AndrogenInsensitivitySyndrome, #SwyerSyndrome, #17BetaHydroxysteroidDehydrogenaseDeficiency, #5AlphaReductaseDeficiency. Males without Y-chromosomes: E.g. #DeLaChapelleSyndrome & very high grades of #CongenitalAdrenalHyperplasia.
Still need to read the CARES Spring Newsletter? View the link below for full access to Vol. 26, and learn more about important research, upcoming events, and more info from our Community! #CARES #CAH #CongenitalAdrenalHyperplasia #CARESFoundation caresfoundation.org/wp-content/upl…
CARES Foundation will be hosting a Parents of CAH Children (Newborn-Age 5) Support Group Meeting next Thursday, April 11, 2024. Please email [email protected] to register for this meeting. #CAH #CARES #Support #CongenitalAdrenalHyperplasia #Advocate
This Wednesday, March 27, 2024, there will be a Spanish Speaking CAH Parents/Patients support group meeting! Please email [email protected] if you are interested in registering! #CARES #Support #SupportGroup #CAH #CongenitalAdrenalHyperplasia
We're so excited to see your for our 30th annual convention! magicfoundation.org/convention/ #GrowthHormoneDeficiency #panhypopituitarism #congenitaladrenalhyperplasia #opticnerverhypoplasia #russelsilversyndrome #smallforgestionalage #cushingsyndrome #mccunealbrightsyndrome
Tomorrow there will be a Support Group Meeting for Parents of Children (Newborn-Age 5) at 9:00PM(ET) on Zoom. Please email [email protected] to register for this meeting! #CAH #Support #CARES #CARESFoundation #CongenitalAdrenalHyperplasia #Newborn #SupportGroups
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1 by Mohammed Ayed Huneif et al. Link : jag.journalagent.com/jcrpe/pdfs/JCR… #Pseudohypoaldosteronism #hyperkalemia #hyponatremia #adrenalcrisis #congenitaladrenalhyperplasia
This Thursday, March 7, 2024, there will be a Support Group Meeting for Parents of CAH Children (School-aged/Teens/Young Adults). Please email [email protected] to register. #CARES #CAH #Support #Advocate #RareDisease #CongenitalAdrenalHyperplasia #SupportGroup
#RareDiseaseDay #congenitaladrenalhyperplasia #CAH #caresfoundation #CAHChampions #RareDisease #CAHparent #CAHpatient #CAHRare
Thank you so much to all who have submitted stories for Rare Disease Day. If you would like to view all of our stories from this week, please visit: caresfoundation.org/rare-disease-d… #CARES #CAH #RareDiseaseDay #RDD2024 #Rare #CongenitalAdrenalHyperplasia #Support #CARESFoundation
Please use the link provided here to access the Cal's full story: caresfoundation.org/wp-content/upl… You can find more stories from Rare Disease Day by visiting caresfoundation.org/rare-disease-d… #CARES #RareDiseaseDay #RDD2024 #CAH #CongenitalAdrenalHyperplasia #Rare #Support #Advocate
Find out about Orlando's story during Rare Disease Day! You can view more stories from the CAH Community for Rare Disease Day by visiting caresfoundation.org/rare-disease-d… #CAH #RareDiseaseDay #CARES #RDD2024 #Rare #Support #CongenitalAdrenalHyperplasia
Get to know more about Zeke's story during Rare Disease Day! You can view more stories from the CAH Community for Rare Disease Day by visiting caresfoundation.org/rare-disease-d… #CAH #RareDiseaseDay #CARES #RDD2024 #Rare #Support #CongenitalAdrenalHyperplasia
Find out more about Marc's story during Rare Disease Day! You can view more stories from the CAH Community for Rare Disease Day by visiting caresfoundation.org/rare-disease-d… #CAH #RareDiseaseDay #CARES #RDD2024 #Rare #Support #CongenitalAdrenalHyperplasia
The full tip sheet can be found at caresfoundation.org/rare-disease-d…. #CAH #RareDiseaseDay #CARES #RDD2024 #Rare #CongenitalAdrenalHyperplasia #Advocate #Support
If you would like to view more CAH Journeys that are a part of Rare Disease Day in 2024, please visit: caresfoundation.org/rare-disease-d… #CAH #CARES #RareDiseaseDay #Rare #CongenitalAdrenalHyperplasia #RDD2024 #Support #Advocate