Congenital Sucrase-Isomaltase Deficiency- CSID
Congenital sucrase-isomaltase deficiency, or c.s.i.d. It's rare congenital disorder of the small intestine, and it's inability to absorb sucrose, you know a common form of sugar. We've all heard of folks who are lactose intolerant. Well c.s.i.d. Is somewhat similar, and can be very very difficult to diagnose.
So here to explain more, as part of our special series behind the mystery, rare and genetic diseases, is Dr. William treem, a pediatric and gastroenterologist. Good morning doctor.
Good morning. Thank you so much for being here. I really appreciate your time. So lets talk about c.s.i.d.
How does it manifest and does it only affect children? no, it doesn't only effect children. Classicaly it does manifest very early in life during infancy with severe diarrhea, bloating gas, abdomonal pain, and poor growth. Malnutrition even. But, it can manifest itself in a less dramatic way, and could effect toddlers, or even older children with what has been called irratable bowel syndrome. Ibs.
But is actually c.s.i.d., or even adolescence, or adults who carry the diagnosis of diarrhea predominate irratable bowel syndrome maybe all their life when in fact they may have had this underlying genetic enzyme defieciency. Which leads me to parents who maybe don't know. And we know it's a genetic disease, it's passed on, and i can only imagine it could be an emotional rollercoaster for parents who are unaware, and their children maybe have the symptoms. They can't really control them, tough right? very tough. Very tough.
And i think the key here is to recognize and be persistent about your childs symptoms. To go to your doctors and make them aware that there is a problem, and that perhaps the remedies that have been suggested are really not doing the trick. But i think that's the key i think. The symptoms are very common. Diarrhea, pain, irratability, but the disease is very rare. Correct. And therefore many physicians are not very familiar with it, and i think it takes the parents to be their childs advocate to really push for the right diagnosis.
And that's why we're talking about it today on the balancing act, and we actually have two families with us we spoke with the harris family earlier today and their journey, and their toddler with c.s.i.d. Let's listen to their story. (music). Well hudson was about four months old when i switched him over from formula from nursing, and within a week he started having huge episodes of explosive diarrhea. 10 to fifteen times a day. We took him to his pediatricians, they ruled out parasites, a virus, they thought he had a milk protein allergy so then they reffered us to several g.i. Specialist that all thought the same thing, so we switched his formula probably nine times, and instead of the symptoms getting better they continued to get worse. Finally we took him to the e.r.
And they said he wasn't leaving the e.r. They did some test and they said he's going to stay and have upper and lower scopes done, and just thankfully the right doctors decided to do the scopes on him really soon and early on, and that's what got us the diagnosis. Well because this is a genetic disease, and both ted and i do not display any symptoms what-so-ever. We're looking into genetic testing for hudson, but also my mom and her twin sister, both have ibs.
So i'm assuming that it could possibly be coming from that side of the family. For us it took nearly five months to get a diagnosis, but once the diagnosis was given to us, and we got him on the medicine, things changed overnight for us, and everything has gotten alot better since then. Now doctor, the harris family very lucky to diagnose this early. Very lucky, because the average time between the onset of symptoms, in this rare disease, and actual diagnosis of the disease is over two years. Oh wow.
So, obviously this family saw the right people, persisted. I know they went through several different diagnosis, but they got to the right diagnosis, and hence hudson is doing extremely well. Well stay right there doctor, because i want to talk more about it, and up next we're going to talk about treatment, finding support, and how one mom's unwavering intuition and determination finally brought about a diagnosis in her daughter. They're going to join us in the studio in just a bit. Stay with us. Welcome back everyone. Joining me now is brandy rayben, and her nine year old daughter addison, who suffers from c.s.i.d., and of course Dr. Treem.
Mom, let me start with you, i know she was diagnosed around two, tell me how you found out. Addison started having symptoms around the age of ten months, she had had a perfectly normal infant childhood, up until ten months, when i started weening her from breast milk, then from ten months to tweny months, she had diarrhea everyday, all day, ten fifteen, up to thirty diapers a day, and. Not normal. Not normal at all.
So, and we started seeing doctors, we were sent to specialist pretty quickly, but unfortunately we went through several doctors and nobody just could believe that really she had that much diarrhea. And thought maybe we were exxagerrating a bit, so we tried different things, got several mis-diagnosis. And finally about twenty months old, she was properly diagnosed through a small bowel biopsy, and we recieved the diagnosis of c.s.i.d. From that point on we she takes medication everyday, she's on a special diet, but otherwise, we've done really well addison is thriving, is very involved with activities, and we have the opportunity to help other families, who are just getting started on the c.s.i.d. Road. And my background is a medical social worker, so i have the opportunity to use my medical social work skills, in addition to real world experience and helping other families and patients who are also dealing with c.s.i.d., and thank goodness you caught it on early, because like the doctor and i were talking, there are so many people that can wait years and years and they don't even know.
Addison let me bring you in, your just, your so darling. Your so beautiful, and i'm glad your doing great. You've obviously had to modify your life, tell me if there is a special diet, the medications, but obviously that's not stopped you. Well i take sucrate with every meal, and i'm on a special diet, but i enjoy riding my bike, and going to school, and doing girl scouts, and dance. So mom she actually just does what every normal child does as long as she takes her medication.
Absolutely her life is not limited by her disorder. And that's awesome. You know doctor it's interesting because she mentioned sucrate, and it really sounds like an easy fix as soon as the diagnosis is there. Yes this is an enzyme replacement therapy. So it replaced the enzyme that's missing in addison's small intestine, and it's an enzyme that comes from bakers yeast. And as long as you take it with every meal, really you can almost completely normalize your diet. There have to be some restrictions, but i think it can make children like addison feel normal, they go to school they participate, they're not afraid of whats going to happen to them. And i think that's been a tremendous advance for us.
And that's the key. The doctor and i were talking about it a few minutes ago, and what your doing. Just creating that awareness right mom. Yes, absolutely.
We know that there are probably under-diagnosed families out there so we just want to build a awareness about c.s.i.d., and so if a patient has ongoing symptoms they can see their physician. I'm going to end with you because your just aboslutely beautiful, and i love you. If someone out there maybe today or tomorrow is maybe finding out that they have c.s.i.d.
What would you tell that child? well, you do have to take medicine everyday, but really you can act normal like any other normal kid. I couldn't have said it better. Thank you so much. Good luck to you. God bless you. Mom thank you so much. Doctor thank you for the information. And if you'd like additional information head to csidcares.org, c.s.i.d.
Patients and caregiver can learn more about support, treatment, education, and much more. Also. Q.o.l. Medical has initiated a research study for children who have been diagnosed with i.b.s., recurring diarrhea, or i.b.s. With current abdomonal pain. To determine whether any of this may actually have c.s.i.d. So that website, check it out, csidgps.com, that's csidgps.com.
Hey it's Marvolo and welcome back to my channel. Today I wanted to tell you all a little bit of a story. And it is about why I stopped being vegan. I was vegan for, I don't…By: Marvolo
Congenital sucrase-isomaltase deficiency, or c.s.i.d. It's rare congenital disorder of the small intestine, and it's inability to absorb sucrose, you know a common form of sugar.…By: TheBalancingAct