Aneal Khan
@anealkhan.bsky.social
MSc (Nutrition), MD, FRCPC (pediatrics), FCCMG (clinical genetics). Rare diseases, genetic, metabolic, gene therapy, innovative therapies. M.A.G.I.C. Clinic, Discovery DNA, Maternal Genomics, Rare Disease Network of Alberta. Calgary, Alberta, Canada.
Hypermobility. Bookings can now be requested for a Core Assessment. Go to hypermobilitycanada.com/hypermobilit... Patients will get a written report to help them move into the next steps of care. #hypermobility #ehlerdanlossyndrome
Hypermobility Canada | Self Referrals
Learn how to self-refer and see our Hypermobility team! Hypermobility Canada is a program designed to support individuals living with hypermobility disorders through personalized, whole-person care.
hypermobilitycanada.com
January 3, 2026 at 3:46 AM
Hypermobility. Bookings can now be requested for a Core Assessment. Go to hypermobilitycanada.com/hypermobilit... Patients will get a written report to help them move into the next steps of care. #hypermobility #ehlerdanlossyndrome
The new M.A.G.I.C. Clinic location in Calgary opens on Monday February 17, 2026. This will be an 8,000 square foot facility focussed on genetic services for rare diseases.
M.A.G.I.C Clinic Canada | HOME
Magic Clinic specializes in metabolics and genetics in Canada. We are a medical clinic that looks after patients with rare diseases due to changes in their DNA.
magiccalgary.ca
January 3, 2026 at 1:32 AM
The new M.A.G.I.C. Clinic location in Calgary opens on Monday February 17, 2026. This will be an 8,000 square foot facility focussed on genetic services for rare diseases.
We have been approached a company to do a clinical trial with a new oral drug in patients with Gaucher disease who have never been on therapy.
Anyone in Canada interested in finding out more can register at viperclinicaltrials.com
Anyone in Canada interested in finding out more can register at viperclinicaltrials.com
December 23, 2025 at 4:13 AM
We have been approached a company to do a clinical trial with a new oral drug in patients with Gaucher disease who have never been on therapy.
Anyone in Canada interested in finding out more can register at viperclinicaltrials.com
Anyone in Canada interested in finding out more can register at viperclinicaltrials.com
Barth syndrome. We have been approached by a company interested in doing a clinical trial in Canada.
If you live in Canada you can register to get more information at viperclinicaltrials.com
If you live in Canada you can register to get more information at viperclinicaltrials.com
VIPeR Home | Viper Clinical Trials
VIPeR is a registry for Canadians who have Rare Diseases or know somebody with a Rare Disease. VIPeR will contact registered members about new clinical trials and research about Rare Diseases.
viperclinicaltrials.com
December 23, 2025 at 4:06 AM
Barth syndrome. We have been approached by a company interested in doing a clinical trial in Canada.
If you live in Canada you can register to get more information at viperclinicaltrials.com
If you live in Canada you can register to get more information at viperclinicaltrials.com
The first gene therapy in the world for Gaucher disease was done here in Calgary. Now we hope to onboard the next study.
December 13, 2025 at 11:40 PM
The first gene therapy in the world for Gaucher disease was done here in Calgary. Now we hope to onboard the next study.
Barth syndrome. Clinical trial proposal in Calgary, Canada. We are trying to see if there are enough patients to start a trial for a new potential therapy here. Sign up to VIPeR for more details.
www.viperclinicaltrials.com
www.viperclinicaltrials.com
VIPeR Home | Viper Clinical Trials
VIPeR is a registry for Canadians who have Rare Diseases or know somebody with a Rare Disease. VIPeR will contact registered members about new clinical trials and research about Rare Diseases.
www.viperclinicaltrials.com
December 11, 2025 at 2:39 PM
Barth syndrome. Clinical trial proposal in Calgary, Canada. We are trying to see if there are enough patients to start a trial for a new potential therapy here. Sign up to VIPeR for more details.
www.viperclinicaltrials.com
www.viperclinicaltrials.com
A new clinical trial for patients with Phenylketonuria (PKU). At MAGIC Clinic in Calgary. viperclinicaltrials.com
December 5, 2025 at 1:12 AM
A new clinical trial for patients with Phenylketonuria (PKU). At MAGIC Clinic in Calgary. viperclinicaltrials.com
Transforming Prenatal Genetics. Special thanks to Pureform for sponsoring this event. See you there tonight.
October 16, 2025 at 2:59 PM
Transforming Prenatal Genetics. Special thanks to Pureform for sponsoring this event. See you there tonight.
The first implementation of Non-Invasive Prental Screening (NIPS) in a community setting in Alberta presented at the CAGC-CCMG meeting in Banff.
October 7, 2025 at 1:38 PM
The first implementation of Non-Invasive Prental Screening (NIPS) in a community setting in Alberta presented at the CAGC-CCMG meeting in Banff.
Private genomic testing in Alberta for a clinical diagnosis. We presented our first round of data at the CAGC-CCMG meeting in Banff. Out of the Public Exomes the yield was 29.41%. Out of the Private exomes the yield was 54.84%. Private labs are providing results that impact health.
October 7, 2025 at 1:37 PM
Private genomic testing in Alberta for a clinical diagnosis. We presented our first round of data at the CAGC-CCMG meeting in Banff. Out of the Public Exomes the yield was 29.41%. Out of the Private exomes the yield was 54.84%. Private labs are providing results that impact health.
#hypermobility #alberta The info session for our new hypermobility program is coming up. Free online or nominal charge in person in Calgary. MAGIC Clinic will be transitioning to this new approach in October. Sign up through Eventbrite at: www.eventbrite.com/e/1549738973...
Hypermobility Canada: Program Launch & Information Session
Join us for the exciting launch of Hypermobility Canada where we will share important information about our new program!
www.eventbrite.com
October 1, 2025 at 1:28 PM
#hypermobility #alberta The info session for our new hypermobility program is coming up. Free online or nominal charge in person in Calgary. MAGIC Clinic will be transitioning to this new approach in October. Sign up through Eventbrite at: www.eventbrite.com/e/1549738973...
End of day2 Ehler-Danlos Scientific Symposium. What I learned - study showing effects of Irbesartan + Celiprolol in vascular EDS - pregnancy management in vEDS - management practices. And our poster on how to optimize genetic testing in hypermobile patients using exomes / genomes.
September 19, 2025 at 1:15 PM
End of day2 Ehler-Danlos Scientific Symposium. What I learned - study showing effects of Irbesartan + Celiprolol in vascular EDS - pregnancy management in vEDS - management practices. And our poster on how to optimize genetic testing in hypermobile patients using exomes / genomes.
Ehlers-Danlos Society 2025 International Scientific Symposium in Toronto. Highlights after the first day:
- a large study of 1000 genomes found no single genetic cause of hypermobility - MTHFR not associated with hypermobility - we presented our poster and study using the FLEx score
- a large study of 1000 genomes found no single genetic cause of hypermobility - MTHFR not associated with hypermobility - we presented our poster and study using the FLEx score
September 18, 2025 at 12:39 PM
Ehlers-Danlos Society 2025 International Scientific Symposium in Toronto. Highlights after the first day:
- a large study of 1000 genomes found no single genetic cause of hypermobility - MTHFR not associated with hypermobility - we presented our poster and study using the FLEx score
- a large study of 1000 genomes found no single genetic cause of hypermobility - MTHFR not associated with hypermobility - we presented our poster and study using the FLEx score
Hypermobility Canada New Program Info Session. Register at: www.eventbrite.com/e/hypermobil...
Hypermobility Canada: Program Launch & Information Session
Join us for the exciting launch of Hypermobility Canada where we will share important information about our new program!
www.eventbrite.com
August 7, 2025 at 4:47 AM
Hypermobility Canada New Program Info Session. Register at: www.eventbrite.com/e/hypermobil...
July 26, 2025 at 4:39 AM
A Phase 2, Randomized, Human Growth Hormone-Controlled, Multicenter,
Basket Study of Vosoritide in Children With Turner Syndrome, Short Stature Homeobox-Containing
Gene (SHOX) Deficiency, and Noonan Syndrome.
If there are patients interested in Canada they can sign up at www.viperclinicaltrials.com
Basket Study of Vosoritide in Children With Turner Syndrome, Short Stature Homeobox-Containing
Gene (SHOX) Deficiency, and Noonan Syndrome.
If there are patients interested in Canada they can sign up at www.viperclinicaltrials.com
VIPeR Home | Viper Clinical Trials
VIPeR is a registry for Canadians who have Rare Diseases or know somebody with a Rare Disease. VIPeR will contact registered members about new clinical trials and research about Rare Diseases.
www.viperclinicaltrials.com
June 6, 2025 at 11:59 PM
A Phase 2, Randomized, Human Growth Hormone-Controlled, Multicenter,
Basket Study of Vosoritide in Children With Turner Syndrome, Short Stature Homeobox-Containing
Gene (SHOX) Deficiency, and Noonan Syndrome.
If there are patients interested in Canada they can sign up at www.viperclinicaltrials.com
Basket Study of Vosoritide in Children With Turner Syndrome, Short Stature Homeobox-Containing
Gene (SHOX) Deficiency, and Noonan Syndrome.
If there are patients interested in Canada they can sign up at www.viperclinicaltrials.com
Vascular malformations, common lymphatic malformations, and KTS/CLOVES syndrome.
We had a site Qualification visit at MAGIC Clinic today for a new clinical trial for patients >= 2 years page age. Sign up for VIPeR to learn more.
www.viperclinicaltrials.com
We had a site Qualification visit at MAGIC Clinic today for a new clinical trial for patients >= 2 years page age. Sign up for VIPeR to learn more.
www.viperclinicaltrials.com
VIPeR Home | Viper Clinical Trials
VIPeR is a registry for Canadians who have Rare Diseases or know somebody with a Rare Disease. VIPeR will contact registered members about new clinical trials and research about Rare Diseases.
www.viperclinicaltrials.com
June 5, 2025 at 11:25 PM
Vascular malformations, common lymphatic malformations, and KTS/CLOVES syndrome.
We had a site Qualification visit at MAGIC Clinic today for a new clinical trial for patients >= 2 years page age. Sign up for VIPeR to learn more.
www.viperclinicaltrials.com
We had a site Qualification visit at MAGIC Clinic today for a new clinical trial for patients >= 2 years page age. Sign up for VIPeR to learn more.
www.viperclinicaltrials.com
May 27, 2025 at 1:12 PM
Non-Invasive Prenatal Screening in Calgary
May 21, 2025 at 1:23 PM
Non-Invasive Prenatal Screening in Calgary
International MPS Day. www.ctvnews.ca/calgary/vide...
International MPS Day
Today is International MPS Day - a series of 7 rare diseases that affect 1 in 25,000 infants in Canada
www.ctvnews.ca
May 16, 2025 at 12:37 AM
International MPS Day. www.ctvnews.ca/calgary/vide...